Co-Expression Analysis of: | CYP73A5, C4H (At2g30490) | Institut de Biologie Moléculaire des Plantes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CYPedia Home | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stress Data Set | save heatmap as: | OpenOffice Table | annotation details for co-expressed genes can be found to the right of the heatmap | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
last updated: | 31/01/06 | MS Excel Table | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
magnitude of change | 0 | 0.3 | 0.6 | 0.9 | 1.2 | 1.5 | 1.8 | 2.1 | 2.4 | 2.7 | >2.99 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
greater than zero | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
less than zero | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Locus | r-value | Name | Description | Agrobacterium tumefaciens, tumor at stem (8) | Myzus persicae, 8h, leaf (82) | Gigaspora rosea, 3d, roots (23) | Heterodera schachtii, 21d, roots (24) | Pseudomonas syringae hrpA, 2h, Col5 leaf (71) | P. syringae DC3000 avrRpm1, 4h, Col5 leaf (71) | P. syringae DC3000, 4h, Col5 leaf (71) | P. syringae hrpA, 4h, Col5 leaf (71) | P. syringae DC3000, 12h, Col5 leaf (71) | P. syringae hrpA, 12h, Col5 leaf (71) | P. syringae DC3000, 2h, Col leaf (106) | P. syringae DC3000, 6h, Col leaf (106) | P. syringae DC3000, 24h, Col leaf (106) | P. syringae avrRpm1, 2h, Col leaf (106) | P. syringae avrRpm1, 6h, Col leaf (106) | P. syringae avrRpm1, 24h, Col leaf (106) | P. syringae HrcC, 2h, Col leaf (106) | P. syringae HrcC, 6h, Col leaf (106) | P. syringae HrcC, 24h, Col leaf (106) | P. syringae pv. phaseolicola, 2h, Col leaf (106) | P. syringae pv. phaseolicola, 6h, Col leaf (106) | P. syringae pv. phaseolicola, 24h, Col leaf (106) | P. syringae, resistant, 4h, Col leaf, uninfected half (148) | P. syringae, resistant, 8h, Col leaf, uninfected half (148) | P. syringae, resistant, 16h, Col leaf, uninfected half (148) | P. syringae, resistant, 24h, Col leaf, uninfected half (148) | P. syringae, resistant, 48h, Col leaf, uninfected half (148) | P. syringae, susceptible, 4h, Col leaf, uninfected half (148) | P. syringae, susceptible, 8h, Col leaf, uninfected half (148) | P. syringae, susceptible, 16h, Col leaf, uninfected half (148) | P. syringae, susceptible, 24h, Col leaf, uninfected half (148) | P. syringae, susceptible, 48h, Col leaf, uninfected half (148) | Erysiphe cichoracearum race UCSC, Col leaf (85) | E. cichoracearum, 3h, Col leaf (86) | E. cichoracearum, 10h, Col leaf (86) | E. orontii, 6h, Col leaf (146) | E. orontii, 12h, Col leaf (146) | E. orontii, 18h, Col leaf (146) | E. orontii, 24h, Col leaf (146) | E. orontii, 48h, Col leaf (146) | E. orontii, 72h, Col leaf (146) | E. orontii, 96h, Col leaf (146) | E. orontii, 120h, Col leaf (146) | Botrytis cinerea, 18h, Col leaf (147) | B. cinerea, 48h, Col leaf (147) | Peronospora parasitica, resistant, 72h (72) | P. parasitica, susceptible, 72h (72) | Phytophtora infestans, 6h, Col seedling (108) | P. infestans, 12h, Col seedling (108) | P. infestans, 24h, Col seedling (108) | elicitor flg22, Ler seedling (81) | elicitor, control MgCl2, 1h, Col leaf (107) | elicitor, control MgCl2, 4h, Col leaf (107) | elicitor, GST, 1h, Col leaf (107) | elicitor, GST, 4h, Col leaf (107) | elicitor, hrpZ, 1h, Col leaf (107) | elicitor, hrpZ, 4h, Col leaf (107) | elicitor, GST NPP1, 1h, Col leaf (107) | elicitor, GST NPP1, 4h, Col leaf (107) | elicitor, flg22, 1h, Col leaf (107) | elicitor, flg22, 4h, Col leaf (107) | elicitor, LPS, 1h, Col leaf (107) | elicitor, LPS, 4h, Col leaf (107) | wounding, 15min, leaf (127) | wounding, 30 min, leaf (127) | wounding, 1h, leaf (127) | wounding, 3h, leaf (127) | wounding, 6h, leaf (127) | wounding, 12h, leaf (127) | wounding, 24h, leaf (127) | wounding, 15min, root (127) | wounding, 30 min, root (127) | wounding, 1h, root (127) | wounding, 3h, root (127) | wounding, 6h, root (127) | wounding, 12h, root (127) | wounding, 24h, root (127) | ozone, 1h, seedling (25) | oxidative stress (paraquat), 30min, leaf (126) | oxidative stress (paraquat), 1h, leaf (126) | oxidative stress (paraquat), 3h, leaf (126) | oxidative stress (paraquat), 6h, leaf (126) | oxidative stress (paraquat), 12h, leaf (126) | oxidative stress (paraquat), 24h, leaf (126) | oxidative stress (paraquat), 30min, root (126) | oxidative stress (paraquat), 1h, root (126) | oxidative stress (paraquat), 3h, root (126) | oxidative stress (paraquat), 6h, root (126) | oxidative stress (paraquat), 12h, root (126) | oxidative stress (paraquat), 24h, root (126) | genotoxic stress (bleomycin), 30min, leaf (126) | genotoxic stress (bleomycin), 1h, leaf (126) | genotoxic stress (bleomycin), 3h, leaf (126) | genotoxic stress (bleomycin), 6h, leaf (126) | genotoxic stress (bleomycin), 12h, leaf (126) | genotoxic stress (bleomycin), 24h, leaf (126) | genotoxic stress (bleomycin), 30min, root (126) | genotoxic stress (bleomycin), 1h, root (126) | genotoxic stress (bleomycin), 3h, root (126) | genotoxic stress (bleomycin), 6h, root (126) | genotoxic stress (bleomycin), 12h, root (126) | genotoxic stress (bleomycin), 24h, root (126) | osmotic stress (mannitol), 30min, leaf (126) | osmotic stress (mannitol), 1h, leaf (126) | osmotic stress (mannitol), 3h, leaf (126) | osmotic stress (mannitol), 6h, leaf (126) | osmotic stress (mannitol), 12h, leaf (126) | osmotic stress (mannitol), 24h, leaf (126) | osmotic stress (mannitol), 30min, root (126) | osmotic stress (mannitol), 1h, root (126) | osmotic stress (mannitol), 3h, root (126) | osmotic stress (mannitol), 6h, root (126) | osmotic stress (mannitol), 12h, root (126) | osmotic stress (mannitol), 24h, root (126) | salt (NaCl), 30min, leaf (126) | salt (NaCl), 1h, leaf (126) | salt (NaCl), 3h, leaf (126) | salt (NaCl), 6h, leaf (126) | salt (NaCl), 12h, leaf (126) | salt (NaCl), 24h, leaf (126) | salt (NaCl), 30min, root (126) | salt (NaCl), 1h, root (126) | sal (NaCl), 3h, root (126) | salt (NaCl), 6h, root (126) | salt (NaCl), 12h, root (126) | salt (NaCl), 24h, root (126) | drought (excised leaves, laminar air flow), 2 h, leaf (58) | drought (15 min dry air, then closed vessels ), 15min, leaf (126) | drought (15 min dry air, then closed vessels ), 30min, leaf (126) | drought (15 min dry air, then closed vessels ), 1h, leaf (126) | drought (15 min dry air, then closed vessels ), 3h, leaf (126) | drought (15 min dry air, then closed vessels ), 6h, leaf (126) | drought (15 min dry air, then closed vessels ), 12h, leaf (126) | drought (15 min dry air, then closed vessels ), 24h, leaf (126) | drought (15 min dry air, then closed vessels ), 15min, root (126) | drought (15 min dry air, then closed vessels ), 30min, root (126) | drought (15 min dry air, then closed vessels ), 1h, root (126) | drought (15 min dry air, then closed vessels ), 3h, root (126) | drought (15 min dry air, then closed vessels ), 6h, root (126) | drought (15 min dry air, then closed vessels ), 12h, root (126) | drought (15 min dry air, then closed vessels ), 24h, root (126) | freezing, recovery, 3h, leaf (58) | freezing, recovery, 24h, leaf (58) | cold (4°C), seedling (76) | cold (4°C), 24h, (58) | cold (4°C), 30min, leaf (126) | cold (4°C), 1h, leaf (126) | cold (4°C), 3h, leaf (126) | cold (4°C), 6h, leaf (126) | cold (4°C), 12h, leaf (126) | cold (4°C), 24h, leaf (126) | cold (4°C), 30min, root (126) | cold (4°C), 1h, root (126) | cold (4°C), 3h, root (126) | cold (4°C), 6h, root (126) | cold (4°C), 12h, root (126) | cold (4°C), 24h, root (126) | heat (30°C), 1h, seedling (59) | heat (40°C), 1h, seedling (59) | heat (55°C), 10min, 1h recovery, suspension cell (26) | heat (38°C), 15min, leaf (126) | heat (38°C), 30min, leaf (126) | heat (38°C), 1h, leaf (126) | heat (38°C), 3h, leaf (126) | heat (38°C), 3h, 1h recovery, leaf (126) | heat (38°C), 3h, 3h recovery, leaf (126) | heat (38°C), 3h, 9h recovery, leaf (126) | heat (38°C), 3h, 21h recovery, leaf (126) | heat (38°C), 15min, root (126) | heat (38°C), 30min, root (126) | heat (38°C), 1h, root (126) | heat (38°C), 3h, root (126) | heat (38°C), 3h, 1h recovery, root (126) | heat (38°C), 3h, 3h recovery, root (126) | heat (38°C), 3h, 9h recovery, root (126) | heat (38°C), 3h, 21h recovery, root (126) | heat (38°C), 15min, suspension cell (126) | heat (38°C), 30min, suspension cell (126) | heat (38°C), 1h, suspension cell (126) | heat (38°C), 3h, suspension cell (126) | heat (38°C), 3h, 1h recovery, suspension cell (126) | heat (38°C), 3h, 3h recovery, suspension cell (126) | heat (38°C), 3h, 9h recovery, suspension cell (126) | heat (38°C), 3h, 21h recovery, suspension cell (126) | UV-B, 15min, leaf (126) | UV-B, 30min, leaf (126) | UV-B, 1h, leaf (126) | UV-B, 3h, leaf (126) | UV-B, 6h, leaf (126) | UV-B, 12h, leaf (126) | UV-B, 24h, leaf (126) | UV-B, 15min, root (126) | UV-B, 30min, root (126) | UV-B, 1h, root (126) | UV-B, 3h, root (126) | UV-B, 6h, root (126) | UV-B, 12h, root (126) | UV-B, 24h, root (126) | high light, leaf (95) | low light, leaf (95) | low light, 3h, petiole (13) | Cs, 7d, leaf (97) | bleomycin, 3d, whole plant (57) | Norfluazone, whole seedling (98) | Zn, whole rosette, A. halleri (101) | Zn, whole roots, A_halleri (101) | Zn, whole rosette, A. petrea (101) | Zn, whole roots, A. petrea (101) | zearalenone (c2t), 14d, seedlings (103) | zearalenone (c4t), 14d, seedlings (103) | Cs, 7d, root (97) | t-zeatin, seedling (115) | fumomisin, protoplast (62) | syringolin, 10h, leaf (86) | isoxaben, suspension cell (10) | Locus | Probeset | Name | Description | Annotation score | GO.keywords | FunCat keywords | AraCyc annotations | KEGG annotations | BioPath annotations | AcylLipid category | Literature annotations | Gene family | 90% quantile of DE | max. DE | |||||||||||||||||||||
At2g30490 | 1.000 | C4H, CYP73A5 | trans-cinnamate 4-monooxygenase / cinnamic acid 4-hydroxylase (C4H) (CA4H) / cytochrome P450 73 (CYP73A5) | 0.4 | -0.1 | 0.1 | 0.6 | 0.6 | 0.8 | 0.4 | 0.4 | 0.4 | 1.4 | 1.3 | -0.7 | 1 | 1 | 0.6 | 1.6 | 1.2 | 0.6 | 1.9 | 1.4 | 1.5 | 2.2 | 0 | 0 | 0 | 0 | -0.2 | 0 | -0.1 | -0.4 | 0.1 | -0.1 | -0.1 | -0.5 | -0.7 | -0.2 | -0.4 | -0.6 | -0.2 | 0 | -0.5 | -0.2 | 0 | -0.1 | 0 | -0.3 | -0.5 | 0.3 | -0.1 | -0.3 | -0.4 | -0.6 | -0.1 | 0.2 | 0.8 | 0.9 | 2.3 | 0.7 | 1.9 | 0.9 | 1.9 | -0.1 | 0.5 | 0 | -0.4 | 0.1 | 0.2 | 0 | 0.1 | 0 | 0 | -0.1 | 0.1 | 0 | -0.1 | 0 | -0.3 | 0.5 | -0.3 | -0.2 | 0 | 0 | 0 | -0.1 | -0.3 | 0 | -0.1 | -0.2 | -0.3 | -0.3 | -0.2 | -0.2 | 0.1 | 0.1 | -0.1 | -0.4 | -0.3 | 0.2 | -0.2 | 0 | -0.2 | -0.1 | -0.3 | -0.1 | 0 | 0.2 | 0.7 | 0.5 | -0.4 | 0 | 0.1 | 0.4 | 0.3 | 0.2 | -0.2 | -0.1 | 0.2 | 0.5 | 0.4 | 0.3 | -0.2 | 0.2 | -0.3 | -0.6 | -0.2 | 0 | -0.3 | 0.2 | -0.1 | 0.1 | 0 | 0 | 0 | -0.3 | 0 | -0.1 | 0.7 | 0 | 0.1 | 0 | -0.4 | 0.7 | 0.4 | 0.2 | 0.6 | 0.1 | 0.2 | 0.3 | 0.8 | -0.3 | -2 | -0.4 | 0 | -0.4 | -0.3 | -0.3 | -0.3 | -0.2 | -1.4 | 0.1 | 0 | -0.4 | -0.7 | -0.4 | 0 | -0.4 | 0 | -0.2 | 0 | -0.5 | -0.1 | -0.7 | -0.2 | -0.6 | 0 | -0.2 | -0.6 | -0.9 | -1.1 | -0.8 | -0.6 | -0.6 | -1.2 | -0.9 | -0.1 | -0.3 | 0.5 | 0.3 | -0.1 | -0.2 | -0.3 | 0 | -0.5 | 0 | 0.7 | 0.5 | -0.2 | -0.2 | -0.3 | -0.7 | -0.3 | 0.2 | 0.8 | -0.3 | 2.3 | -2.4 | 0.5 | -1.8 | -0.6 | -0.4 | -0.1 | 0 | -0.5 | -1.1 | -0.8 | At2g30490 | 267470_at | C4H, CYP73A5 | trans-cinnamate 4-monooxygenase / cinnamic acid 4-hydroxylase (C4H) (CA4H) / cytochrome P450 73 (CYP73A5) | 10 | trans-cinnamate 4-monooxygenase activity | response to light | response to wounding | phenylpropanoid biosynthesis | suberin biosynthesis | lignin biosynthesis | phenylpropanoid pathway, initial reactions | Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | cytochrome P450 family, cinnamic acid 4-hydroxylase, phenylpropanoid metabolism | 2.07 | 4.76 | |||||||||||||||||||||||
At2g40890 | 0.753 | C3'H, CYP98A3 | encodes coumarate 3-hydroxylase (C3H), a P450-dependent monooxygenase. Involved in lignin biosynthesis. | 0.5 | 0 | 0.1 | 0.4 | 0.7 | 0.8 | 0.5 | 0.6 | 0 | 0.7 | 1.2 | -0.4 | 0.1 | 0.7 | 0.4 | 0.2 | 1 | 0.6 | 0.6 | 1.2 | 1.3 | 1 | 0 | -0.1 | 0.1 | 0 | 0.1 | 0 | -0.1 | -0.3 | -0.1 | 0 | -0.2 | -0.1 | -0.4 | 0.1 | 0.2 | 0.1 | 0.1 | 0.2 | 0.1 | 0.3 | 0.2 | -0.1 | 0.1 | -0.2 | -0.6 | -0.5 | 0.2 | -0.1 | -0.2 | -0.4 | -0.1 | 0.3 | 0.4 | 0.9 | 1.3 | 0.4 | 0.9 | 0.9 | 0.9 | -0.1 | 0.2 | -0.3 | -0.4 | -0.1 | -0.2 | -0.1 | 0.1 | 0.1 | 0 | -0.1 | 0 | 0 | 0 | -0.2 | -0.2 | 0.2 | -0.5 | -0.2 | -0.1 | 0 | -0.2 | -0.2 | -0.2 | 0 | -0.1 | -0.2 | -0.1 | -0.3 | -0.2 | -0.2 | 0.1 | 0 | 0 | -0.1 | -0.1 | 0.2 | -0.1 | 0.1 | 0 | 0 | 0 | -0.1 | -0.2 | 0.1 | 0 | -0.4 | -0.4 | 0.1 | 0 | 0.3 | 0.1 | 0.2 | -0.1 | 0 | 0 | 0.1 | -0.2 | -0.5 | -0.3 | -0.1 | -1 | -1.1 | -0.4 | -0.3 | -0.1 | 0.1 | -0.1 | 0 | -0.1 | 0 | 0.1 | -0.1 | -0.2 | -0.2 | 0.6 | 0 | 0.2 | 0 | -0.1 | -0.3 | 0.2 | 0.3 | -0.3 | 0.2 | 0.2 | 0.2 | 0.6 | 0.6 | -1.4 | -0.1 | 0.1 | 0.1 | 0 | 0.3 | 0.4 | -0.7 | -1.2 | -0.4 | 0.1 | -0.1 | -0.4 | -0.5 | -0.1 | -0.3 | 0.1 | 0.1 | 0 | -0.3 | -0.3 | -0.7 | -0.1 | -0.2 | 0 | 0.1 | -0.2 | -0.4 | -0.2 | 0.2 | 0.1 | 0.1 | 0.1 | 0 | 0 | -0.1 | 0.5 | 0 | 0 | -0.1 | -0.1 | 0 | -0.4 | -0.4 | -0.3 | 0 | -0.4 | 0 | -0.4 | 0 | 0 | 0.1 | 0.3 | -0.1 | 3.1 | -2.5 | 0 | -0.8 | -0.5 | -0.4 | -0.2 | 0 | -0.3 | -0.7 | 0.6 | At2g40890 | 245101_at | C3'H, CYP98A3 | encodes coumarate 3-hydroxylase (C3H), a P450-dependent monooxygenase. Involved in lignin biosynthesis. | 10 | p-coumarate 3-hydroxylase activity | monooxygenase activity | phenylpropanoid biosynthesis | lignin biosynthesis | suberin biosynthesis | lignin biosynthesis | phenylpropanoid biosynthesis | Ascorbate and aldarate metabolism | Stilbene, coumarine and lignin biosynthesis | gamma-Hexachlorocyclohexane degradation | Fluorene degradation | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | cytochrome P450 family, 3’-hydroxylase for p-coumaryl shikimic/quinic acids, phenylpropanoid metabolism | 1.38 | 5.69 | |||||||||||||||||||||||
At3g21230 | 0.728 | 4CL4 | 4-coumarate:CoA ligase | -0.7 | 0.6 | -0.1 | -0.1 | 0.5 | 1 | -0.2 | 0 | 2 | 1.8 | 1.1 | -1.2 | 1.7 | 0.8 | 0.6 | 2 | 0.9 | 0.6 | 1.8 | 1.5 | 1.3 | 2.3 | 0.4 | 0.3 | 0.4 | 0 | -0.1 | -0.1 | 0.1 | 0.1 | 0.2 | 0 | -0.1 | -0.5 | -0.5 | -0.4 | -0.5 | -0.5 | -0.2 | -0.4 | -0.6 | -0.6 | -0.5 | 0 | 0.6 | -0.2 | 1.2 | 1.6 | -0.4 | -0.5 | 0 | -0.8 | 0 | 0.2 | 0.6 | 0.8 | 3.3 | 0.5 | 2.5 | 0.9 | 2.3 | -0.3 | 0.3 | -0.5 | 0 | 1.4 | 0 | 0.1 | -0.2 | 0 | -0.5 | 0 | 0.2 | -0.3 | -0.1 | -0.6 | 0.1 | 2.3 | -0.4 | -0.2 | 0 | -0.1 | -0.4 | -0.3 | 0 | 0.2 | -0.6 | -0.4 | -0.2 | 0 | 0 | -0.2 | -0.1 | -0.3 | -0.2 | -0.3 | 0.3 | 0.4 | -0.8 | -0.1 | -0.5 | 0 | -0.1 | -0.1 | 0.4 | 0.3 | 0.4 | 0.9 | 0.1 | 0.6 | -0.2 | 0.5 | 0.1 | 0.5 | 0 | 0 | 0.7 | 0.4 | 0 | 0 | 0.1 | 0.9 | 0.2 | -0.2 | 0 | 0.1 | 0 | -0.4 | 0.1 | 0.2 | 0 | -0.2 | -0.1 | 0 | -0.9 | 1 | 1.5 | -0.4 | 0 | -0.5 | -0.2 | 0.4 | -0.2 | 1.1 | -0.9 | 0.2 | 0.3 | 0.3 | 0 | -1.4 | -1.9 | -0.3 | -0.3 | -0.4 | -0.2 | -0.9 | -0.7 | 0.5 | 0.2 | -0.2 | 0 | 0 | -0.2 | -1.3 | -0.6 | -0.6 | -0.2 | 0.2 | -0.3 | -0.1 | -1 | -1.6 | -0.1 | -0.3 | -0.5 | 0.1 | -0.4 | -0.4 | -1 | -1.1 | -1.2 | -1.2 | -1.4 | -1.1 | -0.6 | 0 | 0 | -1.5 | -0.2 | -0.3 | -0.3 | 0 | 0.1 | -0.1 | -0.2 | -0.6 | -0.7 | -0.5 | -0.2 | -0.2 | -0.2 | 0.6 | 0.1 | -0.8 | 1.8 | -1.3 | -1 | -0.7 | -1.9 | -0.3 | -0.2 | 0.9 | -1 | -0.7 | -0.7 | At3g21230 | 258037_at | 4CL4 | 4-coumarate:CoA ligase | 10 | lignin biosynthesis | flavonoid biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase like | 2.84 | 5.36 | |||||||||||||||||||||||||
At2g37040 | 0.724 | PAL1 | phenylalanine ammonia-lyase 1 | 0.3 | 0 | -0.1 | 0.1 | 0.7 | 0.9 | 0.2 | 0.3 | 0.8 | 1.4 | 1.4 | -0.6 | 1.7 | 1.1 | 0.9 | 1.2 | 1.3 | 0.5 | 2 | 1.5 | 1.3 | 2 | 0.1 | -0.2 | 0 | 0.4 | -0.3 | 0 | 0.1 | -0.5 | 0.3 | 0.2 | -0.3 | -0.5 | -1 | 0.2 | -0.2 | -0.9 | -0.4 | 0 | 0.1 | -0.6 | 0 | 0.2 | 0.1 | 0 | -0.2 | 1.5 | 0.3 | -1.1 | -0.2 | -0.6 | -0.1 | 0.1 | 0.7 | 0.6 | 2.7 | 0.5 | 2.6 | 0.8 | 2.3 | -0.4 | 0.5 | -0.1 | 0 | 0.1 | 0.3 | -0.1 | 0.5 | -0.2 | -0.5 | 0.4 | -0.3 | -0.3 | -0.6 | -0.3 | -0.2 | 1.6 | -0.3 | 0 | -0.1 | -0.5 | 0 | 0.1 | 0 | -0.1 | -0.7 | -0.6 | 0 | -0.3 | -0.6 | -0.6 | 0.3 | -0.4 | -0.5 | -0.6 | 0 | 0 | 0 | -0.3 | -0.1 | -0.4 | 0.2 | 0 | 0.6 | 0.1 | -0.2 | -0.3 | 0.3 | 0.3 | 0.1 | 0 | 0 | 0.2 | 0.1 | 0 | 0.6 | 0.5 | 0 | -0.1 | 0.3 | 0.2 | 0.4 | 0 | 0.2 | 0.3 | -0.6 | 0.2 | 0.2 | 0.4 | 0.4 | -0.3 | 0.1 | -0.4 | -0.3 | 0.6 | 0.9 | 0.3 | -0.2 | 0.1 | -0.3 | 0 | -0.2 | 0.5 | 0.9 | 0.1 | 0.2 | 1.3 | 1.9 | 0.7 | -1.6 | -0.1 | -0.3 | -0.1 | 0 | 0 | 1.2 | -1.1 | -0.2 | 0.9 | -0.6 | -0.8 | -1.5 | -3 | -1.3 | -0.6 | 0 | -0.4 | -0.7 | -0.5 | -1.2 | -2.8 | -1.5 | -1.2 | -0.6 | -0.8 | -0.3 | -0.4 | -0.7 | -1.5 | -1.1 | -1.1 | -1.2 | -0.8 | -0.6 | 0.2 | 0.9 | 0.9 | -0.4 | -0.2 | -0.5 | -0.6 | -0.5 | -0.1 | 1.6 | 0.9 | 0 | 0 | -0.5 | -0.4 | -0.6 | 0.4 | -1 | 0.1 | 0.8 | -0.7 | 0.2 | 0.1 | -0.7 | -0.7 | 0 | 0.4 | -0.5 | -2.7 | -0.6 | At2g37040 | 263845_at | PAL1 | phenylalanine ammonia-lyase 1 | 10 | defense response | response to wounding | phenylpropanoid biosynthesis | phenylalanine ammonia-lyase activity | amino acid metabolism | metabolism of the cysteine - aromatic group | biosynthesis of secondary products derived from L-phenylalanine and L-tyrosine | biosynthesis of phenylpropanoids | salicylic acid biosynthesis | suberin biosynthesis | lignin biosynthesis | phenylpropanoid pathway, initial reactions | Nitrogen metabolism | Tyrosine metabolism | Phenylalanine metabolism | Alkaloid biosynthesis II | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 2.67 | 5.84 | |||||||||||||||||||||||
At3g02360 | 0.723 | 6-phosphogluconate dehydrogenase family protein | 0.5 | 0 | 0 | 0 | 0.4 | 0.8 | 0 | 0 | 0.4 | 0.4 | 1 | -0.5 | 1.1 | 1.1 | 0.6 | 1 | 0.8 | -0.1 | 0.5 | 1.2 | 0.6 | 0.6 | 0 | 0.1 | 0.2 | 0 | -0.1 | 0 | 0 | 0 | 0.1 | 0 | 0.1 | -0.2 | 0 | -0.1 | -0.3 | -0.1 | -0.1 | -0.1 | -0.3 | 0 | 0.1 | 0.7 | 1 | -0.3 | 0.1 | 1.3 | 0.5 | 0.3 | -0.2 | -0.3 | -0.1 | 0 | 0 | 0.9 | 1.3 | 0.8 | 1.3 | 0.9 | 0.5 | -0.2 | 0.1 | -0.1 | -0.3 | -0.2 | 0.1 | -0.1 | 0 | 0 | -0.2 | -0.2 | -0.1 | -0.2 | -0.2 | -0.2 | -0.3 | 0.7 | -0.1 | -0.2 | 0 | 0 | 0 | 0.1 | -0.2 | -0.2 | -0.3 | -0.2 | -0.1 | -0.4 | -0.2 | -0.1 | 0.1 | 0.2 | 0.2 | 0 | -0.3 | -0.1 | -0.4 | -0.1 | -0.1 | 0 | -0.1 | -0.1 | 0.7 | 0.8 | 0.6 | 0.8 | -0.2 | 0 | -0.1 | 0 | 0 | 0 | -0.2 | -0.1 | 0.4 | 0.7 | 0.4 | 0.7 | -0.1 | 0 | -0.4 | -0.6 | -0.3 | -0.3 | -0.3 | -0.1 | 0.1 | 0 | 0.3 | 0.1 | 0.1 | -0.2 | -0.1 | 0 | 0.2 | -0.1 | 0.1 | 0 | -0.1 | 0 | 0 | 0 | 0.1 | -0.1 | -0.1 | -0.2 | -0.3 | -0.6 | -0.5 | -0.3 | -0.3 | -0.3 | -0.5 | -0.4 | -0.1 | -0.6 | -0.3 | 0.3 | 0 | -0.1 | -0.5 | -0.8 | -0.7 | -0.4 | -0.1 | 0 | -0.2 | -0.4 | -0.2 | -0.9 | -0.3 | -0.2 | -0.2 | -0.1 | -0.1 | -0.2 | -0.5 | -0.6 | -0.3 | -0.3 | -0.4 | -0.4 | -0.2 | -0.3 | 0 | 0 | 0 | -0.2 | -0.2 | -0.1 | 0 | -0.6 | 0.5 | 0.6 | 0.1 | -0.2 | 0 | 0 | -0.3 | 0.1 | 0.6 | 0 | 0.5 | -1 | 0 | -0.6 | -0.2 | -0.5 | -0.2 | -0.2 | -0.1 | 0.3 | -0.2 | At3g02360 | 256328_at | 6-phosphogluconate dehydrogenase family protein | 2 | C-compound and carbohydrate metabolism | pentose-phosphate pathway | oxidative branch of the pentose phosphate pathway | superpathway of gluconate degradation | Pentose phosphate pathway | Intermediary Carbon Metabolism | 1.45 | 2.45 | |||||||||||||||||||||||||||
At1g28680 | 0.692 | transferase family protein, similar to elicitor inducible gene product EIG-I24 (Nicotiana tabacum) | 0.2 | -0.1 | 0 | -0.1 | 0.6 | 0.3 | 0.1 | 0.2 | 0 | 0.6 | 1 | -0.9 | 0 | 1.1 | 0.4 | 0.3 | 1.2 | 0.1 | 0.8 | 1.5 | 1.1 | 1 | -0.2 | 0.2 | 0.1 | 0.2 | 0 | -0.3 | -0.1 | 0 | 0.2 | 0.3 | -0.1 | -0.2 | -0.1 | -0.1 | -0.2 | -0.4 | -0.1 | 0 | 0.1 | 0.3 | 0.8 | 0.4 | 0.4 | 0.2 | 0.6 | 0.8 | 0.5 | 1 | -0.3 | -0.5 | -0.1 | 0 | 0.2 | 1 | 1.3 | 0.7 | 1.2 | 1 | 0.3 | -0.5 | 0 | 0.1 | -0.6 | -0.7 | 0.2 | 0 | -0.1 | 0.1 | -0.2 | -0.1 | 0.2 | -0.1 | 0 | -0.3 | 0 | 0 | -0.1 | 0 | 0.1 | -0.1 | -0.2 | 0.1 | -0.2 | 0.2 | -0.2 | -0.3 | 0 | 0 | -0.4 | -0.3 | 0.3 | 0 | 0.1 | 0.3 | -0.1 | 0.4 | 0 | 0.3 | 0.1 | 0.4 | -0.3 | -0.2 | 0.6 | 0.3 | 0.3 | 0.3 | -0.4 | 0.2 | -0.7 | 0 | -0.5 | -0.4 | -0.1 | 0 | 0.3 | 0.1 | 0.1 | 0.1 | -0.2 | 0.8 | -0.3 | -0.9 | -0.8 | -0.7 | -0.1 | 0.3 | -0.1 | 0 | -0.2 | -0.3 | 0.1 | 0.1 | -0.3 | 0 | 1 | -0.3 | 0.3 | 0.1 | 0 | 0.1 | 0 | 0 | 0.5 | 0 | 0 | 0.1 | -0.6 | -0.7 | -1.2 | -0.6 | -0.3 | -0.6 | -0.3 | 0.2 | 0.2 | -1.1 | -0.3 | 0.4 | 0.4 | -0.2 | -0.8 | -0.3 | 0 | -0.3 | 0 | 0.1 | 0 | -0.2 | -0.3 | -1.4 | -0.4 | 0 | 0 | 0.2 | -0.4 | -0.5 | -0.7 | -1.6 | -0.7 | -0.6 | -0.2 | -0.4 | -0.2 | 0.3 | 0.6 | 0 | 0 | 0 | -0.1 | 0.2 | -0.1 | -0.3 | 1.3 | 0.9 | -0.2 | 0 | 0 | -0.1 | -0.3 | -0.6 | 0.2 | -0.1 | 0.8 | -0.7 | 0.6 | -1.1 | -0.6 | 0 | 0 | -0.3 | -0.1 | -1 | -0.7 | At1g28680 | 262744_at | transferase family protein, similar to elicitor inducible gene product EIG-I24 (Nicotiana tabacum) | 1 | acyltransferase, BAHD family, group A, taxol-like | 1.79 | 3.21 | ||||||||||||||||||||||||||||||
At4g20460 | 0.689 | NAD-dependent epimerase/dehydratase family protein, similar to UDP-galactose 4-epimerase from Cyamopsis tetragonoloba and Bacillus subtilis | 1.2 | NA | -0.5 | -1.3 | 1 | 1.2 | 1.1 | 1.4 | 1.8 | 2 | 1.9 | -0.4 | 1.3 | 1.5 | 0.4 | 1.9 | 1.4 | 1.1 | 2 | 2 | 2.9 | 2.2 | 0.2 | 0.1 | 0 | 0.2 | -0.1 | 0 | 0.5 | -0.2 | -0.1 | 0.1 | 0 | 0.1 | -0.5 | -0.7 | -0.2 | -0.8 | -0.6 | -0.3 | -0.2 | -0.7 | 0 | 0.1 | 0.4 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.1 | -0.2 | 0.3 | 0.3 | 0.9 | 1.9 | 3.5 | 1.6 | 3 | 2.1 | 3.7 | -0.6 | 1.4 | -0.1 | -0.5 | 0.1 | 0.1 | 0.3 | -0.2 | -0.2 | -0.1 | 0 | -0.6 | 0 | -0.5 | -0.1 | -0.2 | -0.3 | -0.6 | -0.1 | -0.1 | -0.2 | 0 | -0.3 | -0.3 | -0.8 | -0.2 | -0.3 | -0.6 | -0.8 | -0.8 | 0 | -0.1 | -0.1 | 0 | -0.3 | -0.1 | -0.1 | 0.1 | -0.5 | 0 | 0 | -0.5 | 0 | 0.2 | -0.2 | -0.4 | -0.4 | -0.7 | -1.2 | -0.6 | -1.2 | -1.4 | -1 | -0.3 | -0.2 | 0 | 0 | -0.2 | 0 | -0.9 | -1.4 | -0.2 | -0.3 | -0.3 | 0.3 | -0.3 | -0.2 | 0.6 | 0.5 | 0 | -0.2 | -0.2 | -0.4 | -0.4 | -0.6 | -0.5 | 0 | -0.6 | -0.3 | -0.1 | 0.8 | -0.1 | 0.2 | -0.3 | -0.5 | -0.3 | 0 | 0.1 | 0.1 | -0.2 | 0 | -0.3 | 0.1 | 0.2 | 1 | 1.8 | -0.4 | -0.5 | -0.1 | -0.1 | -0.5 | 0.2 | 0.3 | -0.3 | -0.2 | -0.2 | -0.3 | -0.1 | -0.4 | -1.1 | -1.7 | -0.8 | -0.2 | -0.5 | 0.2 | -0.9 | -0.3 | -0.4 | 0.5 | -0.4 | 0 | 0.1 | -0.6 | 0.2 | -0.1 | -0.6 | 0.1 | 0 | -0.4 | -0.2 | -0.2 | -0.3 | -0.6 | -0.1 | 0 | 0 | -0.3 | -0.2 | -0.2 | -0.2 | -0.2 | -0.4 | -0.5 | 3.2 | -1.9 | -0.9 | -2.9 | -1.3 | -0.2 | -0.7 | -0.3 | 0 | -0.1 | 0.6 | At4g20460 | 254468_at | NAD-dependent epimerase/dehydratase family protein, similar to UDP-galactose 4-epimerase from Cyamopsis tetragonoloba and Bacillus subtilis | 2 | C-compound and carbohydrate utilization | biogenesis of cell wall | GDP-D-rhamnose biosynthesis | colanic acid building blocks biosynthesis | dTDP-rhamnose biosynthesis | galactose degradation I | UDP-glucose conversion | lactose degradation IV | 2.97 | 6.72 | |||||||||||||||||||||||||||||
At4g34050 | 0.685 | CCOMT | caffeoyl-CoA 3-O-methyltransferase | 0.4 | 0.1 | 0.3 | 0 | 0.3 | 0.3 | 0.1 | 0.2 | 0 | 0.9 | 1 | -0.7 | 0 | 0.7 | 0.5 | 0.3 | 0.9 | 0.5 | 0.7 | 1.1 | 0.7 | 0.8 | 0.1 | 0.2 | 0.2 | 0.1 | -0.2 | 0.2 | 0.1 | -0.1 | 0.4 | 0.1 | 0 | -0.1 | -0.2 | -0.4 | 0 | 0 | -0.1 | 0 | -0.1 | -0.1 | -0.1 | 0.2 | 0.3 | -0.3 | 0.2 | -0.4 | -0.1 | 0.2 | -0.1 | -0.1 | 0.2 | 0 | 0.4 | -0.1 | 1 | -0.1 | 0.8 | 0 | 0.8 | -0.2 | 0.5 | -0.1 | 0 | 0 | -0.2 | -0.2 | 0 | 0 | -0.2 | 0.3 | 0 | 0 | 0 | -0.3 | 0 | 0.4 | 0 | 0.1 | 0 | -0.1 | -0.1 | 0 | 0.1 | -0.1 | -0.2 | -0.2 | 0 | 0 | 0 | -0.2 | 0.1 | 0 | -0.1 | 0 | 0.1 | -0.1 | -0.1 | 0.1 | 0 | 0.2 | 0 | 0 | 0.4 | 0.2 | 0.1 | 0.2 | 0.1 | 0 | -0.1 | 0.1 | 0.1 | 0 | 0.2 | 0.2 | 0.6 | 0.7 | 0.4 | 0.6 | 0.1 | -0.1 | -0.6 | -0.9 | 0 | -0.1 | 0.3 | 0 | 0.3 | 0.1 | 0 | 0 | 0 | 0 | -0.4 | 0.1 | 0 | 0 | 0.4 | 0 | 0.1 | 0 | 0 | 0.3 | 0.4 | 0.1 | 0.4 | 0.2 | 0.3 | 0 | -0.6 | 0.1 | -0.1 | 0.2 | 0.1 | 0 | 0.1 | -0.4 | 0 | -0.9 | 0.1 | 0 | -0.6 | -1.5 | -0.4 | -0.2 | -0.1 | 0.3 | -0.3 | 0 | -0.3 | -1.6 | -0.8 | -0.1 | -0.1 | 0 | 0 | -0.4 | -0.8 | -1.6 | -1.3 | -1.4 | -1.6 | -1.4 | 0 | 0.2 | 0.1 | 0.2 | 0 | -0.1 | 0 | 0 | 0.1 | 0 | 0.3 | 0.2 | -0.3 | 0 | 0.1 | 0.1 | -0.5 | 0.1 | 0.4 | -0.2 | 1.6 | -1.3 | 0.2 | -0.2 | -0.5 | -0.5 | 0.1 | -0.2 | -0.2 | -1.3 | -0.3 | At4g34050 | 253276_at | CCOMT | caffeoyl-CoA 3-O-methyltransferase | 10 | biogenesis of cell wall | suberin biosynthesis | lignin biosynthesis | Stilbene, coumarine and lignin biosynthesis | Phenylpropanoid pathway | Methyltransferase, CCOMT like | 1.60 | 3.25 | ||||||||||||||||||||||||
At5g54160 | 0.685 | ATOMT1 | A caffeic acid/5-hydroxyferulic acid O-methyltransferase. Interacts with 14-4-3 proteins in yeast 2 hybrid assay. | 0.3 | 0 | 0.2 | 1.2 | 0.4 | 0.3 | 0.3 | 0.4 | 0.6 | 1.5 | 0.9 | -0.5 | -0.1 | 0.4 | 0.1 | 0.8 | 0.9 | 0.9 | 1.2 | 1 | 1 | 1.2 | 0.1 | 0.1 | 0.1 | 0.2 | -0.4 | 0.7 | 0.2 | -0.6 | 0.1 | -0.1 | -0.4 | -0.3 | -0.4 | 0 | 0.1 | 0.1 | -0.2 | 0.1 | 0 | 0.3 | 0.3 | 0 | 0 | 0 | 0.7 | 0 | 1.2 | 0.3 | -0.1 | -0.3 | 0.1 | 0 | 0.8 | 0 | 1.6 | 0 | 1.8 | 0 | 1.7 | -0.2 | 0.5 | 0 | -0.2 | -0.1 | 0.1 | 0 | 0.9 | 0.2 | -0.3 | 0 | -0.2 | -0.1 | -0.1 | -0.3 | -0.2 | 0.7 | -0.1 | -0.2 | -0.3 | -0.1 | 0 | -0.1 | -0.2 | -0.3 | -0.2 | 0 | 0.2 | 0.2 | -0.7 | -0.5 | -0.2 | -0.7 | -0.3 | -0.7 | -0.2 | -0.3 | -0.4 | 0 | 0 | 0.2 | -0.1 | -0.4 | 0.2 | 0.4 | 1.2 | 0.2 | -0.2 | 0 | -0.1 | 0.3 | 0.4 | 0.5 | -0.1 | -0.2 | 0.4 | 0.8 | 0.9 | 0.2 | 0 | -0.3 | -0.6 | -0.6 | 0.3 | 0 | -0.4 | 0 | -0.2 | -0.2 | -0.1 | -0.2 | 0.2 | -0.3 | -0.4 | -0.4 | -0.3 | -0.5 | 0.2 | -0.2 | -0.2 | -0.1 | 0.9 | -0.2 | -0.5 | -0.1 | 0.3 | 0 | 0.4 | 1 | -1.4 | 0 | -0.1 | 0 | 0 | -0.2 | -0.5 | 0.3 | 0.8 | -0.8 | 0 | -0.3 | -0.3 | -0.7 | -0.7 | -0.3 | 0.6 | -0.1 | 0 | -0.1 | -0.3 | -0.7 | 0 | 0 | 0 | 0 | -0.1 | -0.4 | -0.8 | -1.5 | -1.1 | -1 | -0.6 | -0.8 | -0.2 | 0 | 0 | -0.3 | 0 | 0 | 0.1 | -0.2 | 0 | -0.4 | -0.4 | 0.2 | 0.2 | -0.4 | -1 | 0 | -0.7 | 0 | 0.7 | -0.1 | 1.4 | -1 | -0.6 | -0.2 | -0.6 | -0.2 | 0 | 0 | -0.3 | -1.4 | -1.3 | At5g54160 | 248200_at | ATOMT1 | A caffeic acid/5-hydroxyferulic acid O-methyltransferase. Interacts with 14-4-3 proteins in yeast 2 hybrid assay. | 10 | lignin biosynthesis | caffeate O-methyltransferase activity | suberin biosynthesis | lignin biosynthesis | phenylpropanoid biosynthesis | Flavonoid biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | Methyltransferase, COMT like | 1.83 | 3.38 | |||||||||||||||||||||||
At1g52760 | 0.679 | esterase/lipase/thioesterase family protein, low similarity to monoglyceride lipase from (Homo sapiens, Mus musculus) | 0.6 | 0 | 0.1 | -0.2 | 0.4 | 0.4 | 0 | 0.3 | 0.3 | 0.6 | 1.4 | 0 | 0.8 | 1 | 0.1 | 0.5 | 1.2 | 0.5 | 1.2 | 1.3 | 1 | 1.4 | 0.1 | 0 | 0.2 | 0.2 | 0 | 0 | 0 | 0 | 0.3 | 0 | 0.2 | -0.1 | -0.6 | 0.1 | -0.1 | -0.1 | 0 | 0 | 0 | 0.2 | 0.1 | 0.1 | 0.5 | -0.3 | 0 | 0 | 0.6 | 0.1 | 0 | -0.5 | 0.2 | 0 | 0.7 | 0.4 | 1.1 | 0.1 | 1.1 | 0.5 | 0.7 | -0.1 | 0.6 | -0.1 | -0.2 | -0.4 | 0.2 | 0.1 | 0.3 | -0.1 | -0.2 | 0 | 0 | 0 | 0 | -0.5 | 0 | 0.4 | -0.1 | -0.2 | 0 | 0.2 | -0.1 | -0.1 | 0 | 0 | -0.4 | -0.1 | 0 | -0.1 | -0.2 | -0.2 | -0.1 | 0 | -0.1 | -0.2 | -0.1 | 0.1 | -0.4 | -0.2 | -0.4 | -0.2 | 0 | -0.3 | 0.2 | 0.7 | 0.5 | 0.5 | -0.3 | -0.4 | -0.8 | -0.5 | -0.4 | -0.1 | 0 | -0.1 | 0.1 | 0.7 | 0.3 | 0.2 | -0.4 | -0.4 | -0.9 | -1.5 | -0.6 | -0.5 | -0.3 | 0.3 | 0 | -0.6 | 0.2 | 0.3 | 0.1 | -0.1 | -0.4 | -0.3 | 0.1 | 0 | 0.1 | -0.2 | 0 | -0.2 | 0.3 | 0.2 | -0.2 | 0.3 | -0.3 | 0 | 0.4 | -0.1 | -0.7 | -0.1 | 0 | -0.1 | 0 | -0.5 | -1.1 | -0.5 | -0.4 | 0 | 0.3 | 0 | -0.7 | -0.7 | 0.6 | 0.8 | 0.2 | 0.2 | -0.1 | -0.3 | -0.4 | -0.9 | 0.2 | -0.2 | -0.2 | 0 | 0 | -0.1 | -0.3 | -1.1 | -0.6 | -0.5 | -1 | -0.8 | 0 | -0.3 | 0 | -0.2 | -0.1 | -0.2 | -0.1 | 0.4 | 0 | -0.4 | 0.1 | 1.1 | 0.1 | 0.1 | -0.1 | -0.2 | 0.1 | 0.5 | 0.2 | 0 | 0.5 | -0.9 | 0 | 0.4 | -0.8 | 0.1 | 0 | 0.2 | -0.3 | -2.3 | 0 | At1g52760 | 260153_at | esterase/lipase/thioesterase family protein, low similarity to monoglyceride lipase from (Homo sapiens, Mus musculus) | 2 | Degradation of storage lipids and straight fatty acids | 1.61 | 3.83 | ||||||||||||||||||||||||||||||
At1g48850 | 0.660 | Similar to chorismate synthase from Lycopersicon esculentum | 1.3 | 0 | -0.3 | 0.6 | 0.6 | 0.8 | 0.3 | 0.4 | 0.7 | 0.9 | 1.4 | 0 | 1.1 | 1.1 | 0.4 | 0.9 | 1.1 | 0.3 | 1.1 | 1.3 | 1 | 1.2 | 0.1 | 0 | 0.2 | 0 | -0.4 | 0.2 | -0.2 | -0.1 | 0 | -0.2 | 0 | -0.1 | -0.2 | -0.3 | -0.5 | -0.4 | -0.4 | -0.3 | 0 | 0.5 | 0.5 | 0.7 | 0.9 | -0.6 | 0.3 | 1.5 | 1.2 | 0.2 | -0.4 | -0.5 | -0.1 | 0 | 0.5 | 0.7 | 1.2 | 0.3 | 1.4 | 0.6 | 1.2 | -0.4 | 0.2 | 0 | -0.3 | -0.2 | 0.1 | -0.2 | 0 | -0.3 | -0.1 | -0.2 | -0.2 | -0.3 | -0.2 | -0.2 | -0.2 | 0.9 | 0 | -0.2 | 0.1 | -0.2 | 0 | 0.1 | -0.1 | -0.2 | -0.3 | -0.3 | -0.2 | -0.2 | -0.3 | -0.4 | 0 | -0.3 | 0 | -0.1 | -0.1 | -0.1 | -0.2 | 0.2 | 0 | 0 | 0 | -0.1 | 0.2 | 0.2 | 0 | -0.4 | -0.2 | -0.3 | 0 | 0.1 | -0.3 | -0.1 | -0.1 | -0.3 | -0.4 | -0.2 | -0.1 | 0.1 | -0.3 | -0.4 | -0.8 | -0.8 | -0.5 | -0.4 | -0.4 | 0.2 | 0 | -0.1 | 0.2 | -0.4 | 0 | -0.4 | -0.3 | -0.1 | 0.3 | 0 | 0.4 | 0.1 | 0 | 0 | -1 | 0.6 | 0.7 | 0 | -0.1 | 0 | 0 | -0.2 | -0.4 | -0.3 | -0.3 | -0.2 | -0.2 | -0.3 | -0.1 | -0.6 | 0 | 0.4 | 0 | -0.2 | -0.5 | -0.7 | -0.5 | -0.2 | -0.1 | -0.1 | -0.4 | -0.4 | -0.8 | -1.3 | -0.6 | -0.3 | 0 | 0 | -0.1 | -0.3 | -0.2 | -0.8 | -0.7 | -0.4 | -0.6 | -0.5 | -0.3 | 0 | 0 | 0.5 | -0.1 | 0 | -0.1 | 0.2 | 0 | -0.3 | 1 | 1.1 | 0.2 | -0.3 | -0.5 | -0.6 | -0.4 | 0.1 | 0.6 | 0 | 0 | -0.4 | 0.5 | 0.1 | -0.4 | -0.5 | -0.2 | 0 | -0.3 | 0.2 | -0.1 | At1g48850 | 245832_at | Similar to chorismate synthase from Lycopersicon esculentum | 6 | aromatic amino acid family biosynthesis, shikimate pathway | chorismate biosynthesis | Phenylalanine, tyrosine and tryptophan biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.79 | 2.91 | ||||||||||||||||||||||||||
At3g06350 | 0.660 | dehydroquinate dehydratase, putative / shikimate dehydrogenase, putative | 1.3 | -0.6 | -0.2 | 0.3 | 0.6 | 0.7 | 0.3 | 0.5 | 0.7 | 0.9 | 1.4 | 0.2 | 1 | 1.1 | 0.3 | 0.6 | 1.2 | 0.7 | 0.9 | 1.3 | 1.1 | 1.2 | -0.2 | -0.1 | 0.1 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.1 | -0.2 | -0.1 | -0.3 | 0 | -0.1 | -0.1 | 0 | 0.2 | 0.1 | 0.3 | 0.6 | -0.6 | -0.3 | 0.4 | 0.5 | 0 | -0.1 | -0.3 | 0.2 | 0 | 0.6 | 0.4 | 1.3 | 0.3 | 1.1 | 0.5 | 1.3 | 0 | 0.4 | 0.3 | -0.2 | -0.4 | 0 | 0.4 | 0.2 | 0 | 0.1 | 0 | 0 | -0.2 | 0 | -0.1 | -0.2 | 0.4 | -0.1 | -0.1 | 0 | 0.2 | 0 | -0.1 | 0 | 0 | -0.2 | -0.2 | -0.1 | -0.1 | -0.2 | -0.2 | 0 | 0.2 | 0 | -0.2 | 0 | 0.1 | -0.1 | 0 | 0 | 0 | -0.2 | -0.2 | 0 | -0.1 | -0.4 | -1.3 | -0.3 | -0.1 | -0.3 | -0.2 | -0.5 | -0.3 | -0.2 | -0.3 | -0.4 | 0 | -0.1 | -0.3 | -0.1 | -0.1 | -0.8 | -0.9 | -0.8 | -0.4 | -0.2 | 0.3 | -0.2 | -0.3 | 0 | 0.3 | 0 | -0.4 | -0.1 | -0.2 | 0 | -0.1 | 0.2 | 0 | 0 | 0 | 0.5 | 0.3 | -0.2 | -0.1 | -0.4 | 0.2 | 0.5 | -0.2 | -0.9 | -0.1 | -0.4 | -0.4 | -0.4 | -0.6 | -1 | -0.6 | -0.4 | 0.1 | 0.3 | -0.3 | -0.5 | -0.3 | 0 | 0 | -0.1 | -0.1 | 0.1 | -0.2 | 0 | -0.7 | 0 | -0.2 | 0.1 | 0 | -0.4 | -0.3 | -0.6 | -0.9 | -0.8 | -0.3 | 0 | -0.4 | 0 | 0 | 0.1 | 0.5 | 0.1 | 0 | -0.2 | 0.3 | -0.1 | -0.6 | 0.7 | 1 | 0.2 | -0.1 | -0.2 | 0 | 0 | 0 | -0.5 | 0.6 | 0.6 | -0.8 | -0.8 | 0.5 | 0 | -0.3 | -0.3 | 0 | -0.1 | -0.3 | -0.1 | At3g06350 | 258908_at | dehydroquinate dehydratase, putative / shikimate dehydrogenase, putative | 4 | chorismate biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.75 | 2.78 | ||||||||||||||||||||||||||||
At5g12420 | 0.660 | expressed protein | 2.2 | 0 | -0.4 | -0.8 | 0.8 | 1 | 1.5 | 1.5 | -1 | 1 | 2.1 | -0.8 | -0.2 | 1 | -0.8 | 0.9 | 1.7 | 1.3 | 2.8 | 2.1 | 2.5 | 2.8 | 0.2 | -0.2 | -0.3 | -0.5 | -0.4 | -0.1 | -1.1 | -0.2 | -0.6 | -0.6 | 0.9 | -0.4 | -1.1 | -0.1 | -0.2 | -0.2 | 0 | -0.1 | 0.4 | 0.8 | 1.5 | 0 | -0.6 | 0 | 0.4 | 2.1 | 2.3 | 1.3 | -1 | -0.1 | 0 | 0.3 | 0.3 | 0.7 | 2.4 | 0.1 | 1.9 | 1.1 | 2.8 | 0 | 0.8 | -0.6 | -0.3 | -0.1 | 1 | 1.2 | 0.3 | 0.4 | -0.1 | 0 | 0.2 | 0.1 | -0.1 | -0.2 | 0 | 1 | -0.1 | 0 | -0.2 | 0.1 | -0.3 | 0.4 | -0.1 | 0 | -0.1 | -0.3 | -0.1 | 0 | -0.2 | -0.1 | -0.5 | -0.2 | 0 | 0.1 | 0 | 0.2 | 0.7 | 0.3 | 0.5 | 0.3 | 0.5 | -0.2 | 1 | -0.4 | 0 | 0.1 | -0.6 | -0.2 | 0.9 | 0.7 | 0.7 | 0.2 | -0.3 | 0.1 | -0.4 | -0.5 | -0.5 | -0.7 | -0.4 | -0.1 | -0.6 | -1.7 | 0 | 0.2 | 0.3 | -0.9 | -0.3 | -0.2 | 0.2 | -0.1 | 0.2 | -0.1 | -0.6 | -0.7 | 0 | -0.2 | -0.3 | 0 | -0.2 | 0.3 | 1 | -0.2 | -0.2 | 0 | -0.1 | -0.3 | -0.4 | -0.6 | -0.7 | -0.4 | -0.1 | -0.2 | -0.7 | -1.4 | 0 | -0.3 | -1.4 | 3.2 | -0.4 | 0 | -0.9 | -0.6 | -0.7 | -0.3 | -0.6 | -0.3 | 0 | -0.1 | -0.4 | -0.4 | -0.5 | -0.7 | 0 | 0.1 | -0.1 | -0.7 | -1.4 | -2.1 | -1.5 | -1.5 | -2.4 | -2.2 | -0.4 | -0.2 | -0.1 | 0.4 | 0.1 | 0.1 | 0.6 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | 0.3 | 0 | -0.2 | -0.2 | -0.2 | 0.4 | -0.3 | -0.1 | 2.4 | -2.5 | -1.6 | -1.9 | 0.6 | -0.2 | 0 | -0.4 | 0.4 | -3.6 | -0.2 | At5g12420 | 245181_at | expressed protein | 2 | Fatty acid elongation and wax and cutin metabolism | 3.59 | 6.84 | ||||||||||||||||||||||||||||||
At1g51680 | 0.656 | 4CL1 | encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it also converts ferulate. | -0.2 | 0.1 | 0 | 0.2 | 0.6 | 0.8 | 0.1 | 0.3 | 0 | 0.8 | 0.9 | -0.9 | 0 | 0.6 | 0.3 | 0.3 | 0.9 | 0.4 | 1 | 1.2 | 1.1 | 1.3 | 0 | -0.1 | -0.1 | -0.2 | -0.1 | -0.1 | -0.1 | -0.2 | 0 | 0.1 | 0 | -0.4 | -0.5 | 0.2 | 0 | 0 | 0 | 0 | 0 | 0.4 | 0.3 | 0 | 0.1 | 0 | -0.4 | 0.1 | 0.1 | -0.2 | 0 | -0.5 | 0 | 0.3 | 0.6 | 1.1 | 2 | 0.9 | 1.8 | 1 | 1.2 | 0 | 0.3 | -0.2 | 0 | -0.2 | 0 | 0.1 | -0.3 | 0 | -0.4 | 0.2 | 0.4 | -0.2 | 0.1 | -0.7 | 0 | 0.4 | -0.2 | -0.1 | -0.1 | -0.2 | -0.5 | -0.5 | 0.1 | 0.4 | -0.8 | -0.2 | 0 | 0 | -0.4 | -0.4 | 0.1 | -0.2 | -0.8 | -0.4 | 0.3 | 0.5 | -0.5 | 0.3 | 0 | 0.2 | 0 | 0 | 0.1 | 0.5 | -0.1 | 0.2 | 0 | 0.2 | 0.2 | 1.1 | 0.8 | 1.2 | 0.1 | 0.1 | 0.5 | 0.8 | -0.1 | -0.1 | -0.2 | 0.3 | 0 | 0.7 | 0.7 | 0.8 | 0.1 | 0.3 | 0.1 | 0 | -0.1 | 0.1 | -0.1 | -0.1 | -0.7 | 0 | 1.2 | -0.2 | 0.9 | 0.1 | 0 | 0.1 | 0 | 0.5 | -0.6 | 0.2 | 0.7 | 0.6 | 0.8 | -0.8 | -3.3 | 0 | 0 | -0.3 | 0.1 | -0.8 | -1.2 | -1.4 | -0.2 | 0.2 | 0.1 | -0.2 | -0.9 | -1.6 | -0.3 | 0.1 | -0.1 | -0.1 | -0.4 | 0 | -0.5 | -2.1 | -0.2 | 0 | -0.3 | -0.2 | 0 | -0.2 | -1 | -1.8 | -1.1 | -1.7 | -1.6 | -1.2 | -0.3 | 0.5 | 0.7 | -0.3 | 0 | -0.1 | 0.1 | 0.3 | 0.1 | 0 | 0.7 | 0.9 | -0.6 | -0.3 | -0.2 | 0.2 | -0.3 | 0.3 | -0.5 | -1 | 0.5 | -0.5 | -0.1 | 0.7 | -0.5 | 0.1 | 0.1 | 0.7 | -0.2 | -2.7 | -1 | At1g51680 | 256186_at | 4CL1 | encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it also converts ferulate. | 10 | 4-coumarate-CoA ligase activity | response to UV | response to pathogenic fungi | response to wounding | phenylpropanoid metabolism | lignin biosynthesis | flavonoid biosynthesis | Stilbene, coumarine and lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase | 2.15 | 5.45 | |||||||||||||||||||||||
At5g40760 | 0.642 | Encodes a cytosolic glucose-6-phosphate dehydrogenase that is insensitive to reduction by DTT and whose mRNA is expressed ubiquitously. | 0.9 | -0.3 | -0.3 | 0 | 0.3 | 0.3 | 0 | 0 | 0.5 | 0.7 | 1.7 | -0.4 | 2 | 1.4 | 0.3 | 1.8 | 1.5 | 0 | 1.6 | 1.7 | 0.3 | 1.3 | 0 | 0.4 | 0.9 | 0.9 | -0.3 | 0.2 | 0 | 0.4 | 1.2 | -0.2 | -0.2 | -0.3 | -0.6 | -0.3 | -0.6 | -0.8 | -0.3 | -0.4 | -0.6 | -0.6 | -0.1 | 0.4 | 0.7 | -0.4 | 0.6 | 2.1 | 1.8 | 1.4 | -0.5 | -0.6 | 0 | 0 | 0.3 | 0.3 | 1.1 | 0.3 | 1.2 | 0.3 | 0.3 | -0.4 | 0.1 | 0 | -0.3 | -0.1 | 0.3 | 0.2 | -0.1 | 0 | -0.1 | -0.4 | -0.2 | -0.3 | -0.3 | -0.4 | -0.4 | 1.3 | -0.5 | -0.3 | -0.4 | -0.1 | -0.1 | 0.2 | -0.4 | -0.2 | -0.4 | -0.2 | -0.4 | -0.2 | -0.2 | -0.3 | -0.6 | 0 | 0 | -0.2 | -0.3 | -0.1 | -0.5 | -0.1 | -0.2 | 0 | -0.2 | 0 | 0.9 | 1.2 | 0.6 | 0.8 | -0.5 | -0.3 | -0.1 | 0 | -0.1 | -0.1 | 0 | -0.3 | 0 | 0.8 | 1.1 | 1.8 | -0.4 | -0.3 | -0.8 | -1 | -0.5 | -0.5 | -0.7 | -0.4 | 0 | -0.4 | 0 | 0.2 | 0 | -0.6 | -0.1 | -0.4 | 0 | -0.1 | 0 | -0.3 | -0.3 | 0.1 | 0 | 0.1 | 0.9 | -0.1 | -0.9 | -1 | -0.6 | -0.6 | -0.1 | -0.7 | -0.3 | -0.7 | -0.4 | -0.4 | 0.1 | -0.3 | -0.2 | -0.5 | -0.4 | -0.3 | -0.6 | -0.7 | 0 | -0.2 | 0.3 | -0.1 | -0.1 | -0.5 | -0.1 | -0.1 | -0.4 | -0.2 | 0.1 | -0.1 | -0.3 | -0.3 | -0.1 | 0.4 | 0.2 | 0.2 | 0 | -0.2 | -0.2 | -0.4 | 0 | 0.2 | -0.1 | -0.2 | -0.4 | 0 | -0.1 | -0.5 | 0.8 | 1.8 | 0 | -0.5 | 0 | -0.5 | -0.5 | 0.5 | 0.6 | 0.4 | 3 | -1.9 | -0.4 | -1.6 | -0.4 | -0.5 | -0.5 | -0.4 | -0.1 | -0.4 | -1.9 | At5g40760 | 249372_at | Encodes a cytosolic glucose-6-phosphate dehydrogenase that is insensitive to reduction by DTT and whose mRNA is expressed ubiquitously. | 10 | glucose-6-phosphate 1-dehydrogenase activity | glucose metabolism | pentose-phosphate shunt, oxidative branch | C-compound and carbohydrate utilization | pentose-phosphate pathway | oxidative branch of the pentose phosphate pathway | Pentose phosphate pathway | Glutathione metabolism | Intermediary Carbon Metabolism | 2.18 | 5.01 | ||||||||||||||||||||||||||
At1g22410 | 0.640 | Similar to 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase from Nicotiana tabacum | 0.4 | -1.7 | 0 | 0.4 | 0.5 | 0.7 | 0.2 | 0.1 | 0.6 | 0.8 | 1.1 | -0.6 | 0.5 | 1 | 0.6 | 0.9 | 0.8 | 0 | 0.6 | 1.2 | 0.5 | 0.8 | 0.4 | 0.4 | 0.9 | 0.4 | 0.3 | 0.3 | 0.3 | 0.1 | 0.8 | 0.1 | 0.2 | -0.2 | -0.4 | -0.2 | -0.2 | -0.3 | -0.1 | 0 | 0.2 | 0.5 | 0.8 | 0.6 | 1 | 0 | 0.4 | 0.8 | 0.3 | 0 | -0.3 | -0.3 | 0 | 0 | 0.4 | 0.9 | 1.4 | 0.6 | 1.3 | 0.9 | 1 | -0.3 | 0.3 | 0.1 | 0.1 | 0 | 0.1 | 0 | 0 | 0.1 | -0.4 | 0 | -0.1 | -0.3 | -0.4 | -0.5 | -0.2 | 0.7 | 0 | -0.2 | -0.3 | -0.5 | -0.4 | -0.2 | 0 | -0.1 | -0.3 | -0.4 | -0.2 | -0.2 | -0.4 | -0.6 | 0 | -0.6 | -0.4 | -0.2 | 0 | 0 | -0.4 | 0 | 0 | 0.2 | 0 | -0.2 | 0.4 | 0 | -0.2 | -0.1 | 0 | 0 | 0 | 0.2 | 0 | 0.4 | 0 | -0.3 | 0 | 0.2 | 0 | 0.2 | 0 | 0 | -0.2 | 0.2 | 0.1 | 0.3 | -0.3 | 0.1 | 0 | -0.3 | 0 | -0.5 | -0.1 | -0.1 | -0.5 | 0.2 | 0.5 | -0.1 | 0.3 | 0 | -0.1 | 0.2 | -0.4 | 0 | 0.5 | -0.1 | -0.1 | 0 | 0 | -0.1 | -0.4 | 0 | -0.2 | -0.1 | 0 | 0 | 0.3 | 0 | 0.4 | 0.7 | 0 | -0.2 | -0.9 | -1.6 | -0.9 | -0.4 | -0.2 | 0 | -0.4 | -0.1 | -0.7 | -2.3 | -0.9 | -0.1 | -0.3 | -0.1 | -0.1 | -0.4 | -0.6 | -1.6 | -1 | -0.6 | -0.5 | -0.3 | -0.3 | 0.2 | 0.2 | 0.4 | 0 | -0.2 | 0 | 0 | -0.1 | -0.5 | 0.8 | 0.6 | 0 | 0 | 0.1 | 0.2 | -0.4 | 0.1 | 0.2 | -0.6 | 0.9 | -0.6 | 0.2 | -0.4 | -0.5 | -0.4 | 0 | 0 | -0.3 | -0.8 | -0.9 | At1g22410 | 261933_at | Similar to 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase from Nicotiana tabacum | 6 | aromatic amino acid family biosynthesis, shikimate pathway | homocysteine and cysteine interconversion | Phenylalanine, tyrosine and tryptophan biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.63 | 3.83 | ||||||||||||||||||||||||||
At1g48860 | 0.640 | Strong similarity to 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase from Arabidopsis thaliana | 0.5 | -0.4 | -0.3 | 1.1 | 0.5 | 0.9 | 0.2 | 0.3 | 0 | 0.2 | 1.1 | -0.2 | 0.1 | 0.6 | 0.3 | 0.2 | 0.8 | 0 | 0.3 | 1.1 | 0.7 | 0.5 | 0 | 0.1 | 0 | -0.1 | 0 | 0.1 | 0 | -0.3 | 0 | -0.2 | 0 | -0.1 | -0.3 | 0 | -0.2 | -0.3 | -0.3 | -0.2 | 0 | 0.3 | 0.4 | 0.3 | 0.6 | -0.2 | 0 | 1.2 | 0.3 | 0.2 | -0.4 | -0.4 | 0 | 0 | 0.3 | 0.7 | 1.2 | 0.4 | 1.3 | 0.7 | 1 | -0.5 | 0.4 | 0 | -0.2 | -0.2 | -0.1 | -0.2 | 0.1 | -0.2 | -0.1 | -0.3 | 0 | -0.3 | -0.4 | -0.1 | -0.2 | 0.3 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.1 | 0.1 | -0.3 | -0.2 | -0.1 | -0.2 | 0 | -0.1 | 0.1 | -0.1 | 0.2 | -0.3 | -0.2 | 0.1 | -0.3 | 0 | 0 | 0 | 0 | -0.2 | 0.1 | -0.1 | 0.3 | -0.2 | -0.2 | 0.1 | 0 | 0 | -0.1 | 0 | -0.1 | -0.1 | -0.2 | 0 | 0.3 | 0 | -0.2 | 0.1 | -0.4 | -0.4 | -0.1 | -0.1 | -0.1 | 0.2 | 0.2 | 0 | 0 | -0.3 | 0.2 | -0.5 | -0.1 | -0.1 | 0.4 | 0 | 0 | 0 | -0.1 | 0 | -0.6 | -0.1 | 0.1 | 0 | -0.1 | 0 | 0.2 | 0 | -0.7 | -0.2 | 0 | -0.4 | -0.4 | -0.4 | -0.2 | -0.3 | 0.3 | 0.2 | 0.2 | 0 | -0.3 | -0.8 | 0 | -0.1 | 0.1 | -0.1 | -0.1 | -0.2 | -0.1 | -1 | -0.5 | -0.1 | 0 | 0 | -0.2 | -0.4 | -0.2 | -0.4 | 0 | 0 | 0 | 0 | -0.3 | -0.1 | 0.3 | 0.2 | 0 | -0.1 | -0.2 | 0 | -0.1 | -0.1 | 0.7 | 0.6 | 0.3 | -0.5 | -0.4 | -0.1 | -0.3 | 0.1 | 0.3 | -0.1 | 0 | -0.7 | -0.5 | 0.1 | 0.2 | -0.3 | -0.1 | 0 | -0.3 | 0.3 | -0.1 | At1g48860 | 246627_s_at (m) | Strong similarity to 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase from Arabidopsis thaliana | 6 | glyphosate metabolism | aromatic amino acid family biosynthesis, shikimate pathway | chorismate biosynthesis | Phenylalanine, tyrosine and tryptophan biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.22 | 2.40 | ||||||||||||||||||||||||||
At2g45300 | 0.640 | 3-phosphoshikimate 1-carboxyvinyltransferase / 5-enolpyruvylshikimate-3-phosphate / EPSP synthase | 0.5 | -0.4 | -0.3 | 1.1 | 0.5 | 0.9 | 0.2 | 0.3 | 0 | 0.2 | 1.1 | -0.2 | 0.1 | 0.6 | 0.3 | 0.2 | 0.8 | 0 | 0.3 | 1.1 | 0.7 | 0.5 | 0 | 0.1 | 0 | -0.1 | 0 | 0.1 | 0 | -0.3 | 0 | -0.2 | 0 | -0.1 | -0.3 | 0 | -0.2 | -0.3 | -0.3 | -0.2 | 0 | 0.3 | 0.4 | 0.3 | 0.6 | -0.2 | 0 | 1.2 | 0.3 | 0.2 | -0.4 | -0.4 | 0 | 0 | 0.3 | 0.7 | 1.2 | 0.4 | 1.3 | 0.7 | 1 | -0.5 | 0.4 | 0 | -0.2 | -0.2 | -0.1 | -0.2 | 0.1 | -0.2 | -0.1 | -0.3 | 0 | -0.3 | -0.4 | -0.1 | -0.2 | 0.3 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.1 | 0.1 | -0.3 | -0.2 | -0.1 | -0.2 | 0 | -0.1 | 0.1 | -0.1 | 0.2 | -0.3 | -0.2 | 0.1 | -0.3 | 0 | 0 | 0 | 0 | -0.2 | 0.1 | -0.1 | 0.3 | -0.2 | -0.2 | 0.1 | 0 | 0 | -0.1 | 0 | -0.1 | -0.1 | -0.2 | 0 | 0.3 | 0 | -0.2 | 0.1 | -0.4 | -0.4 | -0.1 | -0.1 | -0.1 | 0.2 | 0.2 | 0 | 0 | -0.3 | 0.2 | -0.5 | -0.1 | -0.1 | 0.4 | 0 | 0 | 0 | -0.1 | 0 | -0.6 | -0.1 | 0.1 | 0 | -0.1 | 0 | 0.2 | 0 | -0.7 | -0.2 | 0 | -0.4 | -0.4 | -0.4 | -0.2 | -0.3 | 0.3 | 0.2 | 0.2 | 0 | -0.3 | -0.8 | 0 | -0.1 | 0.1 | -0.1 | -0.1 | -0.2 | -0.1 | -1 | -0.5 | -0.1 | 0 | 0 | -0.2 | -0.4 | -0.2 | -0.4 | 0 | 0 | 0 | 0 | -0.3 | -0.1 | 0.3 | 0.2 | 0 | -0.1 | -0.2 | 0 | -0.1 | -0.1 | 0.7 | 0.6 | 0.3 | -0.5 | -0.4 | -0.1 | -0.3 | 0.1 | 0.3 | -0.1 | 0 | -0.7 | -0.5 | 0.1 | 0.2 | -0.3 | -0.1 | 0 | -0.3 | 0.3 | -0.1 | At2g45300 | 246627_s_at (m) | 3-phosphoshikimate 1-carboxyvinyltransferase / 5-enolpyruvylshikimate-3-phosphate / EPSP synthase | 10 | glyphosate metabolism | aromatic amino acid family biosynthesis, shikimate pathway | chorismate biosynthesis | Phenylalanine, tyrosine and tryptophan biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.22 | 2.40 | ||||||||||||||||||||||||||
At5g24230 | 0.631 | expressed protein | 0 | 0 | 0.1 | 0 | 0.8 | 1 | 1.1 | 1.3 | 0 | 1.5 | 1.2 | 0 | 0 | 0.8 | 0 | 0 | 1.1 | 1.3 | 1.2 | 0.9 | 1.7 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.6 | 0 | 0.2 | 0.3 | 0.8 | 1.7 | 0.4 | 1.6 | 1.4 | 2 | -0.4 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0 | 0.1 | -0.1 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0.4 | -0.1 | 0 | -0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | 0 | 0.2 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | -1 | -0.9 | -0.9 | -0.6 | -0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.8 | -1.1 | -0.5 | -0.5 | -0.5 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.8 | -0.4 | -0.5 | -0.1 | -0.6 | -0.1 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0.2 | -0.3 | -0.5 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | -0.3 | -0.4 | -0.5 | 0.1 | 0 | -0.4 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | -0.1 | -0.3 | 0 | -0.3 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2.1 | -1.6 | 0 | 0 | 0 | 0 | -0.5 | 0 | 0 | 0 | 0 | At5g24230 | 249779_at | expressed protein | 2 | triacylglycerol degradation | pathogenesis-related lipase like | 1.69 | 3.71 | |||||||||||||||||||||||||||||
At2g47550 | 0.618 | pectinesterase family protein | 4 | -0.7 | -0.3 | 0.3 | 1.2 | 2.1 | 1.4 | 1.4 | 1 | 1.6 | 1.7 | -0.6 | 3.5 | 1.9 | 1.7 | 4.3 | 0.9 | 0.4 | 0.6 | 1.9 | 2.6 | 2.1 | -0.1 | 0 | 0.4 | 0.1 | -0.3 | -0.3 | 0.7 | -0.3 | 0 | -0.7 | -0.2 | -0.4 | -0.2 | -0.5 | -0.7 | -0.5 | -0.7 | -0.1 | 0.1 | -0.7 | -0.3 | 2.3 | 2.6 | -0.3 | -0.1 | 0.9 | -0.1 | -0.7 | 1.3 | -1.2 | -0.5 | 0.7 | 1.2 | 2.3 | 4.2 | 1.6 | 2.5 | 2.3 | 4.2 | -0.6 | 0.7 | -0.3 | 0.1 | 2.3 | 0.7 | 0.7 | 0.2 | 0.3 | -0.6 | 0 | -0.3 | -1 | -0.8 | -0.5 | -0.4 | 0.5 | -1 | 0 | -0.3 | 0 | -1 | -0.3 | -0.3 | -0.3 | -0.7 | -0.7 | -0.3 | -1.3 | -0.3 | 0.2 | -0.6 | -0.2 | -0.7 | -0.3 | -0.3 | -0.4 | -1.2 | -0.7 | -0.7 | -0.4 | -0.4 | 1 | -1 | -0.4 | -0.2 | -0.1 | -0.8 | -1.7 | -2.8 | -1.7 | -1.4 | -0.9 | -0.3 | 0.5 | 0.2 | 0.2 | -0.4 | -0.2 | -1.6 | -1.9 | 0.9 | 2.6 | 1.6 | 2 | -0.5 | -0.5 | -0.1 | 0.5 | -0.5 | -0.3 | -0.2 | 0 | -0.2 | 0.2 | 0.2 | -0.6 | 0.3 | -0.2 | -0.5 | 0.3 | 0.5 | -0.4 | -0.1 | -0.5 | 0.7 | -0.7 | 0 | 0.1 | 0.6 | -0.7 | -0.5 | -0.4 | 0.2 | 0.6 | 0.7 | 0.9 | -0.9 | -1.1 | -0.4 | -0.3 | -0.2 | -0.4 | -0.3 | -0.6 | -0.6 | -0.1 | -1.1 | -0.9 | -1 | -2 | -0.6 | -0.9 | -0.9 | -0.5 | -0.8 | -1 | -1 | -0.1 | 0.3 | 0 | -1.9 | -0.9 | 0.1 | -0.4 | -0.4 | -1.5 | -0.7 | -0.7 | -1 | -0.6 | 0 | 0.4 | -0.5 | -0.5 | -0.3 | 0.1 | -0.3 | -0.2 | -0.8 | 0.1 | -0.5 | -0.6 | 4.3 | -1.9 | 0.2 | -3.3 | -0.5 | -0.1 | -0.4 | 0 | 0 | -0.5 | -2 | At2g47550 | 245151_at | pectinesterase family protein | 2 | Cell Wall Carbohydrate Metabolism | pectin metabolism | 3.83 | 7.73 | ||||||||||||||||||||||||||||||
At5g13420 | 0.615 | similar to transaldolase (Solanum tuberosum) | 0.8 | -0.1 | 0.1 | 0.5 | 0.6 | 0.7 | 0.3 | 0.5 | 0.8 | 1.2 | 1.4 | 0 | 1.2 | 1.1 | 0.6 | 1.4 | 0.9 | 0.7 | 1.4 | 1.4 | 1.1 | 1.3 | 0.2 | 0 | 0.4 | 0.3 | -0.2 | 0.2 | -0.1 | 0 | 0.2 | 0 | 0.1 | 0 | 0 | -0.3 | -0.2 | 0 | -0.3 | -0.3 | -0.1 | -0.1 | 0.2 | 0.8 | 1.4 | -0.2 | 0.7 | 1.4 | 1.3 | -0.4 | -0.2 | -0.2 | 0 | 0 | 0.7 | 0.4 | 1.5 | 0.4 | 1.5 | 0.5 | 1.3 | -0.2 | 0.3 | 0.1 | 0 | 0 | 0.3 | 0 | 0.6 | -0.1 | 0 | 0.1 | -0.5 | -0.4 | -0.5 | 0 | -0.3 | 0 | 0 | -0.2 | -0.1 | -0.1 | 0.2 | 0.5 | 0 | -0.2 | -0.1 | -0.3 | -0.2 | -0.6 | -0.1 | -0.2 | 0 | -0.2 | 0.3 | 0.2 | -0.2 | -0.5 | -0.6 | -0.4 | -0.5 | -0.1 | 0.4 | 0 | 0.2 | 0.1 | 0.6 | 0.2 | 0 | -0.3 | -0.5 | -0.8 | -1 | -0.7 | 0 | -0.2 | -0.4 | 0 | 0.4 | 0.6 | -0.1 | -0.3 | -0.7 | -0.7 | -0.9 | -0.3 | -0.6 | -0.1 | 0.2 | -0.1 | 0 | -0.2 | 0.3 | -0.1 | -0.3 | 0 | -0.2 | -0.2 | -0.2 | 0 | -0.1 | 0.3 | -0.4 | 0.3 | 0 | 0.1 | 0 | -0.1 | -0.1 | 0.1 | -0.2 | 0 | -0.4 | -0.4 | -0.5 | -0.6 | -0.4 | -1 | -0.1 | 0 | 0 | -0.1 | -0.3 | -1.3 | -1 | -0.4 | 0 | 0.3 | -0.1 | -0.2 | -0.9 | -2.1 | -0.9 | -0.1 | -0.1 | 0.1 | 0 | -0.1 | -0.5 | -1 | -0.6 | -0.3 | -0.1 | -0.3 | -0.4 | -0.3 | -0.5 | -0.2 | -0.3 | -0.3 | -0.5 | -0.1 | 0.3 | -0.3 | 0 | 0.5 | 0.4 | -0.1 | -0.1 | -0.3 | -0.5 | 0.3 | 1 | 0.6 | 0.6 | -0.7 | -0.4 | -0.7 | -0.5 | -0.6 | -0.1 | -0.3 | 0 | 0.5 | 0 | At5g13420 | 250234_at | similar to transaldolase (Solanum tuberosum) | 4 | C-compound and carbohydrate metabolism | pentose-phosphate pathway | non-oxidative branch of the pentose phosphate pathway | Pentose phosphate pathway | Intermediary Carbon Metabolism | 2.07 | 3.72 | |||||||||||||||||||||||||||
At2g45290 | 0.614 | strong similarity to transketolase 1 (Capsicum annuum) | 1.4 | -0.4 | -0.2 | 1 | 0.9 | 0.7 | 0.5 | 0.7 | 1 | 1.5 | 1.9 | 0 | 0.6 | 1 | 0.1 | 0.7 | 1.1 | 0.3 | 0.6 | 1.9 | 1.1 | 0.9 | -0.1 | -0.3 | 0 | 0.3 | -0.2 | -0.2 | -0.4 | 0.2 | 0.3 | -0.7 | -0.1 | -0.3 | 0.2 | -0.3 | -0.5 | -0.5 | 0.1 | 0.1 | -0.3 | -0.1 | 0 | 0.6 | 1.2 | 0 | -0.1 | 0.6 | 0.5 | 0.7 | -0.4 | -0.8 | -0.1 | 0 | 0.5 | 1.3 | 1.5 | 1 | 1 | 1 | 1.6 | -0.4 | 0.3 | -0.1 | -0.5 | 0.2 | 0.3 | 0.2 | 0.4 | 0.1 | -0.2 | -0.2 | -0.2 | -0.3 | -0.5 | -0.1 | -0.4 | 0.4 | -0.3 | 0 | -0.1 | -0.2 | 0 | -0.1 | -0.1 | -0.1 | -0.4 | -0.2 | -0.1 | -0.4 | -0.3 | -0.1 | 0.1 | -0.1 | 0.5 | 0.2 | -0.1 | 0 | -0.2 | 0.1 | 0.1 | 0.3 | -0.1 | 0.1 | 0.2 | 0 | 0.4 | 0.2 | -0.1 | -0.2 | -0.4 | -0.8 | -0.9 | -0.3 | -0.2 | -0.1 | 0 | 0.1 | 0.1 | 0.2 | -0.2 | -0.3 | -0.8 | -1 | -1.1 | -0.8 | -0.4 | 0.1 | 0 | 0 | 0.3 | -0.3 | 0.2 | -0.1 | -0.2 | 0 | 0.4 | -0.1 | 0.1 | 0 | -0.2 | 0.2 | 0 | 0.5 | 0 | 0 | -0.1 | -0.3 | -0.9 | -0.5 | -0.7 | -0.1 | -0.2 | -0.4 | -0.4 | -0.7 | -1 | -1 | 0 | -0.2 | 0 | -0.5 | -0.2 | -0.9 | -0.3 | 0.2 | 0.1 | 0.1 | 0 | -0.2 | -0.2 | -1.5 | -0.6 | -0.1 | -0.3 | 0 | -0.2 | -0.5 | -0.6 | -1.2 | -1 | -0.4 | 0 | -0.4 | -0.3 | 0 | 0.2 | 0 | 0 | 0 | -0.4 | -0.3 | -0.1 | -0.1 | 0.4 | 0.5 | 0.1 | -0.5 | 0.2 | -0.2 | -0.2 | 0.4 | 0.6 | 0.3 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.5 | -0.1 | 0.2 | -0.2 | 0.6 | -0.5 | At2g45290 | 245089_at | strong similarity to transketolase 1 (Capsicum annuum) | 6 | C-compound and carbohydrate metabolism | glycolysis and gluconeogenesis | pentose-phosphate pathway | photosynthesis | Calvin cycle | (deoxy)ribose phosphate degradation | ribose degradation | non-oxidative branch of the pentose phosphate pathway | Pentose phosphate pathway | Carbon fixation | Biosynthesis of Polyketides and Nonribosomal Peptides | Biosynthesis of ansamycins | Intermediary Carbon Metabolism | 1.93 | 3.53 | |||||||||||||||||||||||||||
At1g80820 | 0.605 | CCR2 | cinnamoyl CoA reductase isoform 2. Involved in lignin biosynthesis. | 0.9 | -0.5 | -0.4 | -0.7 | 0.5 | 1.4 | -0.6 | -0.5 | 2.5 | 1.9 | 1.1 | -2.2 | 2.3 | 1.6 | 0.8 | 2 | 0.4 | -2 | 2 | 2.1 | 0.5 | 2.4 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.9 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | 0 | 2.4 | -0.5 | -0.5 | 1.9 | -0.5 | -0.5 | 2.3 | -1.5 | -0.3 | 0 | 0 | 2 | 3.3 | 1.7 | 2.6 | 1.7 | 0.9 | -1 | 0 | -0.5 | -0.5 | 1.5 | 0.6 | -0.5 | -0.5 | -0.5 | -1.1 | -0.3 | 0.1 | -0.8 | -0.2 | -1 | -0.3 | 2.7 | -0.5 | -0.5 | -0.5 | -0.5 | 0 | 1.5 | -0.1 | 0.1 | -1 | -0.1 | -0.2 | 0 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | 0.4 | 0.1 | -1.1 | 0.4 | 0 | 0 | -0.5 | 0.5 | 0.5 | -0.5 | -0.5 | 1.4 | 0.4 | 0.8 | 0 | 1.1 | 0.7 | 0.8 | -0.5 | -0.5 | 0.2 | -0.5 | -0.5 | 1 | 0.2 | 2 | 2.1 | 2.7 | 1.2 | 0.7 | -0.5 | -0.5 | 1.4 | 1.1 | -0.5 | -0.5 | -0.5 | -0.5 | -0.8 | 0.9 | 1.9 | -0.7 | 0.5 | -0.5 | -0.7 | 1.8 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.9 | -0.5 | -0.5 | 1.3 | 1.9 | 0.9 | -0.5 | -0.5 | 3.3 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -1 | -0.3 | -0.8 | -1.3 | 0 | -0.3 | -0.8 | -0.6 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.9 | -0.5 | -0.6 | 0.8 | 0.4 | -1.4 | -0.7 | -0.9 | -0.5 | -0.5 | -0.5 | 1.5 | 3.8 | 1.7 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | 4.7 | -3.9 | -0.8 | -4.4 | -0.5 | -0.5 | -0.2 | 0.5 | -0.3 | -0.5 | -3.7 | At1g80820 | 261899_at | CCR2 | cinnamoyl CoA reductase isoform 2. Involved in lignin biosynthesis. | 10 | cinnamoyl-CoA reductase activity | lignin biosynthesis | lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 3.39 | 9.21 | |||||||||||||||||||||||||
At1g80460 | 0.589 | NHO1 | Encodes a protein similar to glycerol kinase, which converts glycerol to glycerol 3-phosphate and performs a rate-limiting step in glycerol metabolism. This gene is required for both general and specific resistance against bacteria and fungi. Arabidopsis | 1 | 0 | 0 | -0.9 | 0.6 | 0.4 | 0.6 | 0.7 | -0.3 | 0.8 | 1.5 | -0.5 | -0.4 | 1.1 | -0.2 | 0.1 | 1.5 | 0.7 | 0.8 | 1.5 | 1.6 | 1.1 | 0 | 0.2 | 0.3 | 0 | 0 | 0 | 0.1 | 0 | 0.3 | 0.2 | 0 | -0.2 | -0.5 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0.4 | 0.6 | -0.4 | -0.5 | -0.3 | 0 | 0 | 0.1 | 0.4 | 0 | -0.2 | 0.2 | 0.4 | 1.1 | 0.9 | 2.2 | 0.5 | 2.2 | 1.2 | 2.3 | -0.1 | 0.5 | -0.2 | -0.3 | -0.3 | 0.1 | 0.2 | 0.1 | 0.5 | 0 | 0 | 0.1 | 0 | 0 | -0.2 | -0.1 | 0.5 | -0.2 | -0.2 | 0 | 0.1 | 0 | 0 | -0.1 | 0.1 | -0.2 | 0 | 0 | -0.2 | 0 | 0.3 | 0 | 0.2 | 0.3 | 0 | -0.2 | 0.1 | -0.1 | 0 | -0.2 | -0.2 | 0.3 | 0 | 0.2 | 0 | -0.6 | -0.4 | -0.2 | 0 | -0.1 | -0.2 | -0.2 | -0.4 | -0.1 | 0 | -0.2 | -0.1 | -0.1 | -0.4 | -0.1 | 0 | -0.5 | -0.6 | -0.3 | -0.4 | -0.2 | -0.7 | 0 | 0 | 0 | 0.1 | 0.1 | 0.3 | -0.5 | -0.1 | 0.1 | -0.1 | 0 | -0.2 | -0.2 | 0 | 1 | -0.7 | -1.9 | -0.2 | -0.1 | -0.6 | -0.1 | -0.2 | -0.9 | -0.2 | 0 | -0.2 | -0.2 | -0.3 | -0.6 | 0.1 | -0.1 | 1.2 | -0.3 | -0.2 | -0.2 | -1.1 | -0.4 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0 | -0.3 | 0.1 | 0.1 | 0 | 0 | -0.2 | -0.2 | -0.5 | -1.1 | -0.9 | -0.9 | -0.5 | -0.3 | -0.2 | -0.3 | 0.2 | 0 | -0.1 | -0.3 | -0.1 | -0.4 | -0.2 | -0.6 | -0.2 | 0.1 | 0 | 0.3 | -0.1 | 0.3 | -0.2 | 0 | 0.1 | -0.2 | 0 | -0.3 | -0.1 | -0.2 | -0.3 | -0.4 | 0 | 0 | 0.1 | -0.4 | -1.3 | At1g80460 | 260274_at | NHO1 | Encodes a protein similar to glycerol kinase, which converts glycerol to glycerol 3-phosphate and performs a rate-limiting step in glycerol metabolism. This gene is required for both general and specific resistance against bacteria and fungi. Arabidopsis | 8 | glycerol kinase activity | response to bacteria | defense response to bacteria | glycerol degradation II | glycerol metabolism | Glycerolipid metabolism | Gluconeogenesis from lipids in seeds | 1.78 | 4.36 | |||||||||||||||||||||||||
At2g45220 | 0.586 | pectinesterase family protein | 2.8 | -0.6 | -0.4 | -0.6 | 1 | 1.7 | 0.7 | 1 | 2.1 | 2.3 | 1.9 | -1.1 | 4 | 4.1 | 1.3 | 5.9 | -0.6 | -0.2 | 4.5 | 2.2 | 2.3 | 5.7 | 2 | 2.5 | 2.4 | 2.4 | -0.6 | -0.6 | 0.5 | 1 | 2.1 | 1.9 | -0.6 | -0.4 | -0.7 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 4 | 2.9 | -3 | 0.9 | 4 | 3.3 | 3.1 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 3.9 | -0.6 | 4.5 | -0.6 | 1.8 | -0.6 | -0.6 | 0.9 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.8 | -0.3 | -0.7 | -0.6 | 0.1 | -0.4 | -0.1 | 2.3 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.5 | -0.2 | -0.9 | -0.1 | 0.1 | 0.2 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.2 | -1 | 0.2 | -0.2 | 0 | -0.6 | -0.6 | -0.6 | -0.6 | 0.8 | 1.4 | -1.1 | -1 | 0.6 | 1.3 | 1.5 | 1.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.3 | -1.1 | -0.2 | -0.6 | 0.9 | 0.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.1 | -0.9 | -1 | -0.2 | 0 | -1 | -0.3 | -0.5 | 0.8 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.8 | -0.6 | -0.4 | -0.1 | -0.4 | -0.8 | -0.6 | -0.6 | 2.9 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.2 | -0.5 | -1 | -1.3 | -0.6 | -0.6 | -0.2 | -0.2 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.1 | -0.9 | -1.2 | -1.4 | -0.7 | -0.9 | -0.4 | 1.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 1.7 | -0.9 | 0.8 | 5.4 | -2.5 | 0.3 | -6.1 | -3 | 1.9 | -0.7 | -0.9 | -0.6 | 1.2 | -4.6 | At2g45220 | 245148_at | pectinesterase family protein | 2 | Cell Wall Carbohydrate Metabolism | pectin metabolism | 4.38 | 12.08 | ||||||||||||||||||||||||||||||
At3g21240 | 0.585 | 4CL2 | encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it does NOT convert ferulate. | 1.2 | 0 | 0 | 0.9 | 0.5 | 1.1 | -0.3 | 0 | 0.2 | 0.7 | 1.1 | -0.6 | 1 | 0.8 | 0.6 | 1.6 | 0.3 | 0.3 | 1.2 | 1.1 | 1.6 | 1.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.3 | 0 | 0 | -0.5 | -0.4 | 0 | -0.5 | -0.1 | -0.1 | -0.2 | -0.2 | -0.3 | 0.3 | 0.3 | 0 | 0 | 0.5 | 0.3 | 0.1 | -0.3 | -0.1 | 0 | 0.2 | 0 | 0.6 | 0.7 | 0.6 | 0.8 | 0.9 | 0 | 0.1 | 0 | -0.3 | 0.4 | 0.2 | -0.1 | -0.2 | -0.2 | 0.5 | 0.1 | 0.1 | 0.3 | 0 | 0.1 | -0.5 | -0.1 | 0.7 | -0.1 | -0.3 | -0.1 | -0.5 | -0.3 | 0.1 | 0 | 0.2 | -0.5 | -0.1 | 0.1 | -0.2 | 0.1 | 0.2 | -0.4 | -0.4 | -0.5 | -0.3 | 0 | 0.4 | -0.5 | 0 | -0.2 | -0.1 | 0.1 | 0 | 0.9 | 0.4 | 0.5 | 1.3 | -0.1 | 0.1 | -0.5 | 0.2 | 0 | 0 | 0.1 | 0 | 0.8 | 0.5 | 0.2 | 0.8 | 0 | 0.1 | -0.9 | -0.9 | -0.3 | -0.5 | 0 | -0.5 | 0.7 | 0.5 | 0.1 | -0.2 | -0.1 | 0.1 | -0.1 | 0 | 0.8 | 0 | 0.6 | 0 | 0 | -0.1 | 0 | 0.3 | -0.6 | 0.6 | 0 | 0 | -0.1 | -0.7 | -0.2 | -0.1 | 0.1 | -0.1 | 0.1 | -0.5 | -1 | -1 | 0.1 | 0 | -0.2 | 0 | -0.1 | -0.1 | -0.1 | -0.5 | 0.1 | 0.2 | 0 | -0.1 | -0.8 | -2.1 | -0.2 | 0.1 | 0 | 0.1 | -0.2 | -0.3 | -0.7 | -2.4 | -2.3 | -1.6 | -1.1 | -1.4 | 0 | 0 | 0.5 | -0.5 | 0 | -0.1 | -0.4 | 0 | 0.2 | 0 | 0 | 0 | -0.8 | -0.4 | 0 | 0 | -0.4 | 0.8 | -0.2 | -0.9 | 1.3 | -1.4 | 0.3 | 1.6 | -0.2 | -0.9 | -0.2 | 0.1 | -0.6 | -0.1 | 0.1 | At3g21240 | 258047_at | 4CL2 | encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it does NOT convert ferulate. | 10 | 4-coumarate-CoA ligase activity | response to UV | response to pathogenic fungi | response to wounding | phenylpropanoid metabolism | suberin biosynthesis | lignin biosynthesis | flavonoid biosynthesis | Stilbene, coumarine and lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase | 2.04 | 4.27 | |||||||||||||||||||||||
At4g35150 | 0.583 | O-methyltransferase family 2 protein, similar to caffeic acid O-methyltransferase, Pinus taeda | 0.9 | 0 | -0.1 | -1.1 | -0.1 | 0.6 | -0.3 | -0.3 | 1.6 | 0.9 | 2.1 | -0.3 | 4.8 | 2 | 2.4 | 3 | 0.7 | -0.3 | 3.7 | 2.1 | 0 | 2.1 | 0.8 | -0.2 | 0.1 | 0.2 | -0.6 | 0.5 | 0.4 | -0.7 | 0 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | -0.1 | -0.1 | 0.6 | 2.5 | -0.1 | -0.1 | -0.8 | -0.1 | 0.4 | -0.5 | -0.1 | 0.7 | 0.2 | 0 | -0.1 | 1.7 | 0.2 | 1.4 | 0.3 | 1.6 | 0.4 | 0.9 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.4 | 0.1 | 0 | -0.2 | -0.4 | -0.1 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.2 | -0.1 | -0.4 | 0 | -0.6 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | -0.3 | 0 | 0.2 | -0.1 | -0.1 | -0.1 | 1.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.4 | 0 | -0.2 | -0.5 | -1.4 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.1 | -0.9 | -1.4 | -0.4 | -1.7 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.7 | -0.1 | -0.3 | 0.1 | -0.1 | 0.4 | 0 | 1.7 | -0.1 | 1.3 | 0.9 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | 0.1 | -0.1 | 0.5 | 0.2 | 0.2 | -1.4 | 1.1 | -0.1 | -0.1 | -0.1 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.5 | -1.1 | -2.6 | -2.1 | -0.5 | -0.5 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.5 | 0 | -0.3 | -0.7 | -0.7 | -0.4 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.9 | -0.6 | -1.5 | 2.9 | -3.6 | -0.3 | -2.5 | 0.3 | -0.9 | 0 | 0.8 | -0.1 | -0.4 | -0.1 | At4g35150 | 253177_s_at (m) | O-methyltransferase family 2 protein, similar to caffeic acid O-methyltransferase, Pinus taeda | 2 | Phenylpropanoid pathway | Methyltransferase, COMT like | 2.79 | 8.50 | |||||||||||||||||||||||||||||
At4g35160 | 0.583 | O-methyltransferase family 2 protein, similar to caffeic acid O-methyltransferase, Pinus taeda | 0.9 | 0 | -0.1 | -1.1 | -0.1 | 0.6 | -0.3 | -0.3 | 1.6 | 0.9 | 2.1 | -0.3 | 4.8 | 2 | 2.4 | 3 | 0.7 | -0.3 | 3.7 | 2.1 | 0 | 2.1 | 0.8 | -0.2 | 0.1 | 0.2 | -0.6 | 0.5 | 0.4 | -0.7 | 0 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | -0.1 | -0.1 | 0.6 | 2.5 | -0.1 | -0.1 | -0.8 | -0.1 | 0.4 | -0.5 | -0.1 | 0.7 | 0.2 | 0 | -0.1 | 1.7 | 0.2 | 1.4 | 0.3 | 1.6 | 0.4 | 0.9 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.4 | 0.1 | 0 | -0.2 | -0.4 | -0.1 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.2 | -0.1 | -0.4 | 0 | -0.6 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | -0.3 | 0 | 0.2 | -0.1 | -0.1 | -0.1 | 1.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.4 | 0 | -0.2 | -0.5 | -1.4 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.1 | -0.9 | -1.4 | -0.4 | -1.7 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.7 | -0.1 | -0.3 | 0.1 | -0.1 | 0.4 | 0 | 1.7 | -0.1 | 1.3 | 0.9 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | 0.1 | -0.1 | 0.5 | 0.2 | 0.2 | -1.4 | 1.1 | -0.1 | -0.1 | -0.1 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.5 | -1.1 | -2.6 | -2.1 | -0.5 | -0.5 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.5 | 0 | -0.3 | -0.7 | -0.7 | -0.4 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.9 | -0.6 | -1.5 | 2.9 | -3.6 | -0.3 | -2.5 | 0.3 | -0.9 | 0 | 0.8 | -0.1 | -0.4 | -0.1 | At4g35160 | 253177_s_at (m) | O-methyltransferase family 2 protein, similar to caffeic acid O-methyltransferase, Pinus taeda | 2 | Phenylpropanoid pathway | Methyltransferase, COMT like | 2.79 | 8.50 | |||||||||||||||||||||||||||||
At4g36220 | 0.578 | FAH1, F5H, CYP84A1 | encodes ferulate 5-hydroxylase (F5H). Involved in lignin biosynthesis. | -1.1 | 0 | 0.5 | 0 | 0.2 | 0.1 | 0.2 | 0.2 | 0.1 | 1.1 | 1.1 | -0.4 | -0.7 | 0.8 | 0 | 0.7 | 1.3 | 1 | 0.4 | 1.2 | 0.8 | 1 | -0.1 | 0.4 | 0 | 0 | -0.9 | 0 | -0.6 | -0.2 | 0 | 0 | 0 | -0.1 | 0 | 0.2 | -0.3 | -0.2 | -0.1 | 0 | 0 | 0.2 | 0.6 | 0.4 | 1.2 | -0.1 | 0.5 | 1.6 | 2.4 | 1.2 | -0.7 | 0 | 0.4 | 0.2 | 0.7 | 0.2 | 1.4 | 0 | 1.4 | 0.4 | 1.3 | 0.5 | 0.6 | -0.1 | -0.3 | -0.8 | 0.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.3 | 0 | 0.1 | 0 | 0 | -0.1 | -0.5 | -0.3 | 0 | 0.1 | 0.1 | 0 | 0 | -0.2 | 0 | -0.5 | -0.1 | 0.1 | -0.2 | -0.2 | 0.1 | 0.1 | -0.2 | 0 | -0.4 | 0 | -0.4 | -0.1 | -0.1 | 1.1 | 1.2 | 0.7 | 0.9 | 0 | 0 | 0 | 0 | 0 | 0 | -0.2 | -0.2 | -0.1 | 0 | -0.8 | -0.7 | 0 | 0 | -0.2 | 0 | 0 | -0.2 | -0.7 | 0.3 | 0 | -0.3 | 0 | 0 | 0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.5 | 0.2 | 0.4 | 0.3 | 0 | -0.1 | 0 | 0.1 | -0.7 | -1.2 | 0 | 0 | 0 | 0 | 0 | 0 | -1.2 | -2.2 | 0 | 0 | 0.1 | -1 | -1 | -0.8 | 0 | -0.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | -0.3 | -0.1 | -0.4 | -0.5 | 0.7 | 0.8 | 0.3 | -1.1 | 0.1 | -0.5 | 0.4 | 0.2 | 0 | 3.3 | -2.4 | -2 | -2.4 | -2 | -0.4 | -0.7 | 0.6 | 0.1 | -1.9 | 0 | At4g36220 | 253088_at | FAH1, F5H, CYP84A1 | encodes ferulate 5-hydroxylase (F5H). Involved in lignin biosynthesis. | 10 | monooxygenase activity | ferulate 5-hydroxylase activity | lignin biosynthesis | phenylpropanoid biosynthesis | biosynthesis of secondary products derived from L-phenylalanine and L-tyrosine | biosynthesis of phenylpropanoids | biogenesis of cell wall | lignin biosynthesis | Ascorbate and aldarate metabolism | Stilbene, coumarine and lignin biosynthesis | gamma-Hexachlorocyclohexane degradation | Fluorene degradation | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | cytochrome P450 family, 5-hydroxylase for coniferaldehyde, coniferyl alcohol and ferulic acid, phenylpropanoid metabolism | 2.26 | 5.77 | ||||||||||||||||||||||
At1g06550 | 0.577 | Enoyl-CoA hydratase/isomerase family protein | 1.4 | -0.1 | 0 | 0.9 | 0.9 | 0.8 | 0.2 | 0.5 | 0.3 | 0.2 | 1.1 | 0.2 | 0.6 | 0.4 | 0.3 | 1.2 | 0.5 | 0.1 | 0.7 | 0.9 | 1 | 0.9 | 0 | 0 | -0.2 | -0.2 | 0 | 0 | 0 | -0.2 | -0.2 | -0.1 | -0.2 | 0 | -0.7 | -0.2 | -0.4 | -0.1 | 0 | 0 | 0 | -0.4 | -0.6 | 0 | -0.5 | -0.1 | -0.3 | -0.5 | -0.3 | -1.3 | -0.1 | -0.1 | 0.2 | 0 | 0.5 | 0.8 | 1.3 | 0.3 | 1.3 | 0.8 | 1 | 0 | 0.2 | 0.3 | -0.1 | -0.4 | 0 | 0.2 | -0.2 | -0.4 | -0.2 | -0.1 | 0 | -0.1 | 0 | -0.3 | -0.1 | 0 | 0.3 | 0.1 | 0 | 0 | -0.1 | -0.3 | 0 | 0.1 | -0.2 | -0.1 | 0 | -0.1 | 0.1 | -0.3 | 0.1 | 0 | -0.3 | -0.1 | 0 | 0 | -0.1 | 0.2 | 0.1 | 0.1 | 0 | 0 | -0.1 | 0 | -0.5 | -0.7 | -0.1 | 0 | -0.1 | 0.3 | 0 | 0.6 | 0.1 | -0.1 | -0.3 | 0.1 | -0.6 | -0.5 | 0 | 0 | -0.7 | -0.6 | -0.4 | -0.2 | 0.1 | 0.5 | 0.1 | 0 | 0 | -0.3 | -0.1 | -0.3 | 0 | -0.1 | 0.3 | 0.2 | 0.7 | 0.3 | 0 | -0.5 | -0.6 | 0.4 | 1.2 | 0.5 | -0.2 | 0.5 | 0.5 | -0.8 | -1.7 | 0 | 0 | -0.2 | -0.2 | -1 | -1.2 | -0.5 | 0.3 | 0.3 | 1.1 | 0 | -0.9 | -1.4 | 0.3 | 0.2 | 0.4 | 0.3 | 0.2 | -0.1 | -0.4 | -1.6 | 0 | -0.1 | 0.9 | 0.2 | -0.4 | -0.9 | -0.4 | -1.1 | -1 | -0.7 | 0 | 0 | -0.1 | 0.1 | 0.5 | 1.9 | 0.2 | 0 | -0.2 | 0.4 | -0.4 | -0.3 | 1.2 | 0 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.4 | -0.2 | 0.3 | 0 | 0 | 0 | 0 | -0.4 | 0.4 | 0 | 0.3 | 0 | -2 | 0 | At1g06550 | 262619_at | Enoyl-CoA hydratase/isomerase family protein | 2 | valine degradation II | valine degradation I | 1.90 | 3.97 | ||||||||||||||||||||||||||||||
At2g46500 | 0.569 | phosphatidylinositol 3- and 4-kinase family protein / ubiquitin family protein | 0.4 | -0.2 | -0.2 | -0.7 | 0.2 | 0.3 | 0 | 0.1 | 0.7 | 0.5 | 0.3 | -0.3 | 1.6 | 0.3 | 0.4 | 1.2 | 0.2 | 0 | 0.5 | 0.4 | 0.7 | 1 | 0 | 0 | 0.1 | -0.1 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0 | -0.1 | 0.3 | -0.2 | -0.3 | 0 | 0 | -0.2 | -0.3 | -0.3 | -0.3 | 0.3 | 0.4 | -0.3 | -0.6 | 0.8 | 0 | -0.1 | 1.1 | -0.6 | 0 | 0 | 0.2 | 0.4 | 1.3 | 0.2 | 1.5 | 0.3 | 1.1 | -0.4 | 0.1 | 0.8 | 0.9 | 0.9 | 0 | 0.1 | -0.1 | -0.1 | -0.2 | -0.2 | -0.1 | -0.2 | -0.3 | 0 | -0.2 | 1 | -0.1 | -0.1 | -0.5 | -0.2 | -0.4 | -0.2 | -0.3 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.5 | -0.3 | -0.4 | 0 | -0.1 | -0.3 | -0.2 | -0.3 | -0.2 | -0.1 | 0 | -0.2 | -0.3 | 0 | 0.3 | 0.5 | 0.3 | 0.2 | 0 | 0.1 | 0.2 | 0.3 | 0.6 | 0.4 | -0.2 | -0.5 | -0.1 | 0.2 | -0.2 | -0.1 | 0 | 0 | 0.4 | 0.9 | 0.7 | 0.4 | -0.2 | -0.3 | -0.1 | 0.1 | -0.2 | 0 | -0.2 | -0.6 | 0 | 0 | 0 | -0.3 | -0.2 | -0.3 | -0.4 | 1.3 | 0 | 0 | -0.5 | -0.5 | -0.3 | 0 | 0.5 | -0.2 | 0 | -0.4 | -0.3 | -0.5 | -0.1 | 0 | 0.6 | 0.7 | -0.1 | -0.1 | -0.2 | -0.8 | -0.6 | -0.4 | 0 | -0.1 | -0.2 | -0.4 | -0.2 | -0.4 | -0.2 | -0.1 | 0 | -0.6 | 0 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.4 | -0.5 | -0.5 | -0.4 | -0.1 | -0.2 | -0.1 | -0.1 | -0.2 | -0.1 | -0.2 | 0 | -0.1 | 0.4 | 1.4 | 1.2 | -0.2 | -0.3 | 0 | -0.2 | -0.2 | 0 | -0.2 | 0 | 1.6 | -1 | -0.9 | -1.3 | 0 | 0 | -0.2 | -0.5 | -0.2 | 1.3 | -1.1 | At2g46500 | 265461_at | phosphatidylinositol 3- and 4-kinase family protein / ubiquitin family protein | 2 | Lipid signaling | 1.67 | 2.91 | ||||||||||||||||||||||||||||||
At2g17130 | 0.556 | IDH2 | NAD+ dependent isocitrate dehydrogenase subunit 2 (IDH2) | 0.9 | -0.2 | 0 | -0.5 | 0.2 | 0.4 | 0.6 | 0.6 | 0.8 | 0.4 | 0.8 | -0.2 | 1 | 0.8 | 0.2 | 1.5 | 1 | 0.3 | 1.3 | 0.9 | 0.6 | 1.2 | 0.1 | 0.2 | 0.7 | 0.4 | -0.2 | 0 | 0 | 0.5 | 0.7 | 0.1 | 0.5 | -0.2 | -0.3 | -0.2 | -0.4 | -0.1 | -0.2 | 0 | 0 | 0.2 | 0.5 | 0.7 | 0.7 | -0.1 | 0.5 | 1.1 | 0.4 | 0.9 | -0.5 | 0 | 0.1 | -0.1 | 0.3 | 0 | 0.9 | 0 | 1.1 | 0.3 | 1.1 | -0.1 | 0.3 | -0.2 | 0 | -0.2 | 0 | 0 | -0.2 | 0.5 | -0.2 | -0.1 | -0.3 | -0.1 | -0.3 | -0.4 | -0.2 | 0.6 | 0.3 | 0 | -0.3 | -0.2 | -0.3 | 0.3 | -0.2 | -0.2 | 0.1 | -0.2 | -0.2 | -0.4 | 0.1 | 0 | -0.5 | -0.1 | 0.2 | 0.8 | -0.2 | -0.2 | -0.1 | -0.3 | -0.1 | 0 | -0.1 | 0 | 0.7 | 0.3 | 0.4 | 1.1 | -0.3 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0 | -0.1 | -0.5 | 0 | 0 | 0.6 | -0.1 | -0.2 | -0.2 | -0.3 | -0.3 | -0.3 | 0.4 | -0.5 | 0.2 | -0.3 | 0 | -0.1 | -0.1 | 0.3 | -0.3 | -0.3 | -0.5 | -0.2 | -0.3 | -0.2 | -0.2 | 0 | -0.4 | 0.3 | 0.2 | -0.2 | -0.4 | -0.1 | -0.6 | -0.6 | 0.6 | -0.1 | -0.2 | -0.1 | -0.3 | -0.2 | -0.3 | -0.9 | -0.5 | 0.6 | -0.7 | -0.1 | -1.2 | -1.3 | -1.4 | -0.8 | -0.5 | -0.3 | -0.4 | -0.4 | -0.4 | -0.7 | -0.9 | -0.4 | -0.8 | -0.5 | -0.4 | -0.5 | -0.2 | -0.5 | -0.2 | -0.3 | 0 | -0.4 | 0 | -0.1 | -0.1 | -0.3 | -0.1 | -0.2 | -0.1 | 0.3 | 0.2 | 0 | 1.4 | 1.3 | 0.5 | 0.9 | 0 | -0.2 | 0.1 | 0.5 | 0.9 | 0.6 | 2.3 | -1.9 | -1.6 | -0.7 | -0.8 | 0.1 | -0.2 | -0.9 | -0.1 | 0 | -1.4 | At2g17130 | 263583_at | IDH2 | NAD+ dependent isocitrate dehydrogenase subunit 2 (IDH2) | 4 | C-compound and carbohydrate metabolism | tricarboxylic-acid pathway (citrate cycle, Krebs cycle, TCA cycle) | leucine biosynthesis | TCA cycle variation VIII | TCA cycle variation IV | TCA cycle -- aerobic respiration | Citrate cycle (TCA cycle) | Intermediary Carbon Metabolism | 1.88 | 4.29 | |||||||||||||||||||||||||
At1g15950 | 0.555 | CCR1 | Cinnamoyl CoA reductase isoform 1 (CCR1). Involved in lignin biosynthesis. | 0.1 | 0.1 | 0.1 | 0.2 | 0.5 | 0.2 | 0.1 | 0.2 | 0 | 0.5 | 0.5 | -0.2 | 0.6 | 0.3 | 0.7 | 0.2 | 0.5 | 0.5 | 0.4 | 0.7 | 0.6 | 0.2 | 0.2 | 0.2 | 0.4 | 0.1 | 0 | 0.3 | 0.2 | 0.3 | 0.3 | 0.2 | 0 | -0.1 | -0.5 | -0.1 | 0 | -0.1 | 0 | 0 | -0.2 | -0.3 | 0 | 0.1 | 0.1 | 0 | 0.5 | -0.1 | 0.3 | -0.1 | 0 | -0.3 | 0 | -0.3 | 0.2 | -0.2 | 0.2 | -0.3 | 0 | -0.1 | 0 | -0.4 | 0 | 0 | -0.1 | 0 | -0.1 | 0 | 0.3 | 0 | 0 | 0 | 0.1 | -0.1 | 0.3 | 0.2 | 0 | 0.3 | -0.1 | 0 | 0 | 0.1 | 0.1 | 0 | 0.1 | 0.1 | -0.1 | 0.1 | 0 | 0 | -0.3 | -0.1 | 0.1 | 0.2 | 0.2 | 0 | 0.1 | 0.2 | -0.1 | 0.4 | 0.2 | 0.4 | 0 | -0.1 | -0.1 | -0.3 | -0.1 | -0.3 | -0.3 | -0.2 | -0.6 | 0.2 | 0.3 | 0.7 | 0 | 0 | 0 | 0.6 | 0.2 | 0.1 | 0 | 0 | -0.8 | -0.3 | 0 | 0 | 0.1 | 0.2 | 0.3 | 0 | 0 | -0.1 | 0.2 | 0 | -0.2 | 0.1 | 0.4 | -0.1 | 0.4 | 0 | -0.1 | -0.4 | 0 | 0.3 | 0.6 | 0.2 | 0 | 0.1 | 0.6 | 0.6 | -1.5 | 0 | 0 | 0 | 0 | -0.6 | -0.9 | -0.7 | -0.1 | -0.3 | 0.1 | 0.2 | -0.6 | -1.1 | -0.6 | -0.5 | 0.1 | 0 | 0 | 0 | -0.2 | -0.7 | 0.3 | 0.1 | 0.3 | 0 | -0.2 | -0.2 | -0.4 | -0.2 | -0.2 | -0.1 | -0.1 | -0.4 | -0.2 | 0 | 0.3 | -0.4 | 0.1 | -0.1 | 0 | 0 | 0 | -0.1 | 0 | 0.1 | 0 | -0.1 | -0.3 | 0.2 | -0.8 | 0.3 | 0.7 | 0.3 | 0.8 | -1.5 | -0.2 | -0.2 | -0.2 | -0.5 | 0 | 0 | -0.3 | -1 | -1.1 | At1g15950 | 261792_at | CCR1 | Cinnamoyl CoA reductase isoform 1 (CCR1). Involved in lignin biosynthesis. | 10 | cinnamoyl-CoA reductase activity | lignin biosynthesis | lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 1.26 | 2.38 | |||||||||||||||||||||||||
At5g64100 | 0.555 | peroxidase, putative | 0 | -0.5 | 0.2 | -1.3 | 0.7 | 1 | 1.5 | 2.4 | 1.6 | 3 | 0 | 0 | 1.4 | 0 | 0 | 0 | 0 | 2 | 2.4 | 0 | 2.4 | 4.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.7 | 0 | 0 | 0 | 0 | 0 | 0.7 | 0 | 0 | 0 | 2.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.8 | 0 | 0.3 | 0.1 | 0.1 | -0.1 | 0 | 0 | -0.5 | 0.4 | 0.4 | 0.8 | 0 | 0 | 0.6 | 0 | -0.1 | 0.3 | 0 | 0.2 | -0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | -0.1 | 0.2 | -0.3 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | -0.5 | -0.9 | -1.3 | -1.3 | -0.7 | -0.7 | 0 | 0 | 0.6 | 0 | 0 | 0 | -0.6 | -1.1 | -1 | -1.1 | -0.8 | -0.4 | -0.7 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.6 | -0.1 | -0.3 | 0 | -0.2 | -0.3 | -0.5 | 0 | 0 | -0.8 | -1.2 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.2 | 0 | 0 | 0.5 | 0.7 | 1 | -0.3 | 0 | 0 | 0 | 0 | 0 | -0.8 | 0 | 0 | 0 | 0 | -0.3 | -0.2 | 0 | 0.2 | -0.5 | -0.2 | 0 | -0.2 | -1 | -1 | -1.8 | 0 | 0.3 | -0.7 | -1.4 | 0.2 | -0.4 | -0.2 | -0.2 | -0.3 | -0.6 | -0.1 | 0 | 0.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.8 | 1.6 | 0.3 | 4.6 | -2.2 | -0.4 | -3.8 | -0.6 | -0.2 | -0.2 | 0.4 | 0 | 0 | -2.3 | At5g64100 | 247297_at | peroxidase, putative | 2 | disease, virulence and defense | detoxification | Methane metabolism | Prostaglandin and leukotriene metabolism | Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis | 2.58 | 8.68 | |||||||||||||||||||||||||||||
At5g39580 | 0.553 | peroxidase, putative | 0.2 | -0.2 | -0.5 | -0.5 | 0.7 | 1.5 | 1.5 | 1.6 | 2.5 | 3 | 1.2 | -0.3 | -0.7 | 1.9 | 0 | 2.5 | 1.7 | 2.2 | 2 | 0.9 | 2.8 | 3.8 | -0.1 | -0.2 | -0.4 | -0.4 | -0.3 | -0.8 | -0.2 | -0.4 | -0.3 | 0.4 | -0.4 | -0.8 | -0.2 | -0.8 | -0.2 | -0.4 | -0.5 | -0.5 | -0.1 | -0.8 | -0.3 | -0.1 | 0 | 0.5 | 0 | 3.2 | 0.9 | -0.4 | 3.1 | -0.9 | -0.1 | 1.1 | 2.3 | 1.8 | 5.4 | 1.6 | 4.9 | 2.1 | 4.1 | -0.8 | 0.6 | 1.6 | 0.5 | 1 | -0.8 | 1 | 2.9 | 1.4 | -1.3 | -0.1 | 0 | -1.2 | -0.1 | 0.4 | -0.4 | 2.3 | -1.3 | -1.1 | -1.7 | -1.3 | -0.1 | 0.7 | -0.1 | 0 | -1 | 0.1 | 0.2 | -1.1 | -1 | -0.8 | -1.9 | -1.1 | -0.3 | -0.1 | 0.1 | 0.2 | -2.4 | 0.2 | 0.6 | -0.8 | 1.1 | -0.8 | -1.5 | -1.3 | 0 | 0.1 | 0.1 | 1 | -0.7 | 1.2 | 1.7 | 0.5 | -0.4 | -0.7 | -1 | -1.2 | -0.5 | -0.1 | 0.1 | 1.2 | 1.4 | 3.6 | 2.7 | 2.3 | -1.4 | -1 | -0.7 | 0.5 | -2 | -1.2 | -0.7 | 0 | -0.3 | 0.4 | 1 | -0.3 | 1 | -0.4 | -1.1 | -0.1 | 0.9 | -0.6 | -2 | -2.2 | -0.4 | -0.2 | -0.6 | -0.4 | -0.1 | -1.3 | -0.5 | -1.2 | 1.1 | 2.7 | 2.3 | 3.4 | -0.5 | 0.2 | -1.4 | -2.4 | 0.1 | -1.1 | -1.4 | -1.5 | -0.4 | 0 | -1.5 | -1.2 | -1.5 | -1.4 | 0 | -0.6 | -1.5 | -1 | -0.8 | -0.9 | -1.2 | -1.1 | -0.4 | -2 | -2.5 | -1.1 | -1 | 0 | 0.8 | -2.1 | -1.3 | -1.1 | -0.8 | 0 | 0.8 | 0.3 | -1.7 | -1.7 | -1 | 0.4 | 0 | -0.4 | -0.2 | -0.3 | 0.4 | -0.6 | 3.1 | -2.2 | 0.6 | -3.7 | -0.4 | -1.1 | 0.1 | -1.7 | -0.4 | -0.8 | -0.5 | At5g39580 | 249459_at | peroxidase, putative | 2 | Methane metabolism | Prostaglandin and leukotriene metabolism | Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis | 4.75 | 9.18 | ||||||||||||||||||||||||||||||
At3g57550 | 0.549 | AGK2 | guanylate kinase | 1.4 | -0.4 | -0.4 | 0.3 | 0.2 | 0.8 | 0.5 | 0.8 | 1.7 | 1.3 | 0.6 | -0.9 | 1.5 | 1.1 | 0.7 | 1.8 | 0.9 | 0.8 | 1.5 | 1.2 | 1.7 | 1.4 | 0.1 | 0 | 0.7 | 0.5 | 0.1 | -0.2 | 0.2 | 0.2 | 1.2 | 0.3 | -0.2 | 0 | 0.6 | -0.5 | -0.3 | -0.8 | -0.6 | -0.2 | -0.1 | -0.1 | 0.6 | 0.5 | 0.9 | -0.6 | 0.3 | 1.4 | 0.5 | -0.7 | 0.2 | -0.6 | 0.1 | 0 | 0.8 | 1.1 | 2.7 | 1.1 | 2.5 | 1.4 | 1.6 | -0.7 | 0.4 | -0.3 | -0.2 | 0 | -0.2 | -0.6 | -0.2 | 0 | -0.5 | -0.5 | -0.5 | -0.6 | -0.5 | -0.7 | -0.5 | 0.6 | 0 | 0 | -0.5 | -0.6 | 0.1 | 0.4 | -0.4 | -0.4 | -0.4 | -0.5 | -0.5 | -0.4 | -0.3 | 0.2 | 0.1 | -0.1 | 0.7 | 0.1 | -0.5 | 0.1 | 0.5 | 0.2 | 0 | 0 | 0 | -0.4 | 0.2 | 0 | 0.9 | 1.2 | -0.2 | 0 | 0 | 0 | -0.1 | 0 | -0.5 | -0.5 | -0.5 | -0.6 | -0.5 | -0.2 | -0.3 | 0 | -0.2 | -0.4 | -0.3 | -0.3 | -0.9 | -0.2 | -0.4 | 0.1 | -0.6 | -0.9 | -0.1 | -0.5 | -0.2 | -0.4 | -0.2 | -0.4 | -0.3 | -0.4 | -0.3 | -0.2 | -0.2 | 0.8 | -0.6 | -1 | -0.5 | 0.2 | 0.5 | -0.1 | 0.7 | -0.5 | -0.4 | -0.3 | -0.4 | -0.4 | -0.2 | 0.7 | -0.7 | 0.3 | -0.8 | -1.1 | -1 | -0.6 | -1 | -0.2 | -0.3 | -0.4 | -0.7 | -0.4 | 0.2 | 0.2 | -0.8 | -0.5 | -0.6 | -0.6 | -0.3 | -0.1 | 0.1 | 0.1 | 0 | -0.1 | 0 | 0 | -0.4 | -0.5 | -0.3 | -0.5 | -0.5 | -0.5 | -0.5 | -0.5 | -0.4 | 0.6 | 1.7 | 1.1 | 0 | 0 | -0.5 | -1 | -0.1 | 0 | -0.3 | 0.2 | -0.1 | -0.7 | -0.6 | -0.1 | -0.5 | -0.4 | 0 | -1 | 0.2 | 1.9 | -0.7 | At3g57550 | 251643_at | AGK2 | guanylate kinase | 6 | nucleotide metabolism | purine nucleotide metabolism | de novo biosynthesis of purine nucleotides I | Nucleotide Metabolism | Purine metabolism | 2.25 | 3.94 | |||||||||||||||||||||||||
At4g30190 | 0.548 | AHA2 | belongs to the P-type ATPase superfamily of cation-transporting ATPases, pumps protons out of the cell, generating a proton gradient that drives the active transport of nutrients by proton symport. | 2 | -0.1 | 0.4 | -1.1 | 0.6 | 0.5 | 0.8 | 0.9 | 0.5 | 1.3 | 1.3 | 0 | 0.9 | 1.2 | 0.3 | 1.2 | 1.4 | 0.9 | 2 | 1.2 | 1.1 | 2 | 0 | -0.1 | -0.4 | -0.1 | -0.2 | 0.1 | 0 | -0.4 | -0.3 | 0 | 0.4 | -0.1 | -0.6 | 0.1 | 0 | 0.1 | -0.2 | 0 | 0.1 | 0.5 | 0.6 | 0 | 0.6 | 0.2 | 0.9 | -0.3 | -0.2 | -0.4 | -0.2 | 0.1 | 0.2 | 0.1 | 0.6 | 0.1 | 1.4 | 0.1 | 1.5 | 0.2 | 1.6 | 0.2 | 0.6 | 0.6 | -0.1 | 0 | 0.4 | 0 | 0.1 | 0.9 | 0 | 0.1 | 0 | 0.1 | 0 | 0 | 0 | -1.1 | 0 | -0.1 | 0.3 | 0 | 0.1 | 0.6 | -0.1 | 0.1 | 0.2 | -0.1 | 0 | -0.1 | 0 | -0.1 | 0 | -0.3 | 0 | 0.5 | -0.2 | 0 | 0 | 0 | -0.1 | 0.1 | 0.2 | -0.3 | -0.4 | -2.3 | -1 | -0.3 | -0.1 | -0.3 | -0.6 | -0.4 | -0.5 | -0.4 | 0 | -0.1 | -0.9 | -0.8 | -0.3 | 0.7 | 0 | -0.1 | -1.2 | -1.2 | -0.5 | -0.4 | -0.1 | 1.1 | 0.4 | -0.2 | -0.5 | -0.5 | -0.1 | 0.2 | 0 | -0.1 | -0.3 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | 0.5 | 0.4 | -0.1 | 0.2 | -0.7 | -0.1 | -0.5 | -1 | 0.3 | 0 | 0 | 0 | -0.1 | -0.1 | -0.3 | -1.2 | -0.1 | 0.4 | 0.6 | 0.2 | -0.7 | -1.8 | -0.5 | 0 | 0 | 0.3 | 0 | 0 | -0.2 | -0.5 | -0.2 | -0.2 | -0.1 | 0 | -0.4 | -0.6 | -1 | -0.9 | -0.5 | -0.9 | -0.6 | -0.2 | -0.1 | -0.1 | -0.1 | -0.3 | -0.1 | -0.3 | 0 | 0.5 | 0.2 | -0.9 | -0.9 | -0.4 | -0.4 | 0.2 | -0.3 | 0.2 | 0.3 | 0 | 0 | 0 | 2.2 | -1.4 | -0.4 | -0.3 | -0.3 | -0.4 | 0 | 0.2 | -0.2 | -2.5 | 0.5 | At4g30190 | 253609_at | AHA2 | belongs to the P-type ATPase superfamily of cation-transporting ATPases, pumps protons out of the cell, generating a proton gradient that drives the active transport of nutrients by proton symport. | 9 | hydrogen-exporting ATPase activity, phosphorylative mechanism | nutrient import | transport facilitation | transport ATPases | eukaryotic plasma membrane / membrane attached | Oxidative phosphorylation | 2.33 | 4.77 | ||||||||||||||||||||||||||
At5g48930 | 0.546 | HCT | Hydroxycinnamoyl-CoA:shikimate/quinate hydroxycinnamoyltransferase | -0.2 | 0 | 0.2 | 0.3 | 0.3 | 0.6 | 0.1 | 0.2 | -0.2 | 0.8 | 0.6 | -0.9 | -0.5 | 0.3 | 0.5 | -0.2 | 0.6 | 0.3 | 0.5 | 0.7 | 0.7 | 0.5 | -0.2 | -0.2 | -0.3 | -0.2 | -0.2 | -0.2 | -0.1 | -0.4 | -0.2 | -0.2 | 0 | -0.2 | -0.4 | 0 | 0.1 | 0 | -0.1 | 0.1 | 0.2 | 0.2 | 0.3 | -0.3 | 0 | 0 | 0.4 | -0.4 | 0.3 | -0.3 | -0.4 | -0.3 | 0 | 0 | 0.5 | 0 | 1 | 0 | 0.8 | 0.1 | 0.7 | 0 | 0.3 | -0.3 | -0.3 | 0.1 | -0.2 | -0.4 | -0.1 | -0.2 | 0.1 | 0.1 | 0.4 | 0 | 0.1 | 0 | 0.1 | 0.6 | -0.4 | 0 | 0.4 | 0.1 | 0 | -0.1 | 0.1 | 0.2 | -0.2 | 0 | 0 | 0.1 | -0.2 | 0 | 0.4 | 0 | -0.3 | -0.6 | 0.2 | 0.5 | -0.2 | 0.3 | -0.1 | 0.1 | -0.2 | -0.1 | -0.1 | -0.3 | -0.2 | -0.6 | 0 | 0.5 | 0.1 | 0.4 | 0.4 | 0.7 | 0 | 0.2 | 0.2 | 0.1 | 0 | -0.2 | -0.1 | 0.5 | -0.2 | -0.1 | 0.3 | 0.4 | 0.2 | 0.3 | 0.2 | 0.3 | -0.2 | -0.1 | 0 | -0.1 | -0.2 | 0.2 | 1.2 | 0.1 | 0.5 | 0 | 0 | 1.4 | 0.6 | -0.1 | -0.6 | 0.1 | 0.4 | 0.3 | 0.8 | 0.4 | -0.4 | -0.1 | 0 | -0.1 | 0 | 0.4 | 0.9 | -1 | -0.2 | -0.3 | 0.2 | 0.3 | -0.2 | 0.3 | 0 | -0.2 | -0.1 | 0 | 0 | 0 | -0.3 | -0.9 | 0.1 | 0 | -0.1 | 0 | -0.1 | -0.2 | -0.8 | -0.9 | -0.5 | -0.6 | -0.7 | -0.3 | -0.2 | 0.1 | 0.5 | -0.3 | 0 | -0.2 | -0.1 | 0 | -0.6 | -0.6 | 0 | 0.2 | -0.7 | -0.6 | -0.7 | 0.4 | -0.1 | 0 | -1.3 | -0.6 | 1 | -0.6 | 0.7 | -0.7 | -0.2 | -0.5 | -0.1 | 0.2 | 0 | -2.4 | 0 | At5g48930 | 248639_at | HCT | Hydroxycinnamoyl-CoA:shikimate/quinate hydroxycinnamoyltransferase | 10 | Phenylpropanoid pathway | acyltransferase, BAHD family, group D, HCT | 1.44 | 3.88 | |||||||||||||||||||||||||||
At1g02500 | 0.545 | SAM1 | S-adenosylmethionine synthetase gene sam-1 | -0.1 | 0 | 0.3 | -0.5 | 0.2 | 0.4 | 0.1 | 0.2 | 0.6 | 0.4 | 0.9 | 0 | 0.4 | 0.7 | 0.3 | 0.2 | 0.5 | 0.2 | 0.9 | 0.9 | 0.6 | 0.9 | 0 | 0.1 | 0.2 | 0.1 | 0 | 0 | 0 | 0 | 0.5 | 0 | 0.2 | 0 | 0.1 | -0.1 | -0.1 | -0.1 | 0 | 0 | 0 | 0.1 | 0.2 | 0.1 | 0.2 | -0.1 | 0.3 | 0.6 | 0.3 | 0.4 | -0.2 | 0 | 0 | 0 | 0.4 | 0 | 1 | 0 | 1.1 | 0 | 0.7 | 0 | 0.2 | -0.1 | -0.1 | -0.1 | 0 | -0.2 | 0.1 | 0 | 0 | 0 | -0.2 | -0.2 | -0.1 | 0 | -0.1 | 0.4 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | 0 | -0.2 | -0.1 | -0.1 | 0 | -0.2 | 0.1 | 0.1 | 0.2 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.3 | 0.1 | -0.1 | 0 | -0.2 | 0.3 | 0.1 | -0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0.2 | 0.6 | 0.6 | 0 | -0.1 | -0.8 | -0.8 | -0.5 | -0.5 | -0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0 | 0.3 | 0.3 | 0 | 0.1 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0.9 | 0.3 | -0.3 | 0 | 0 | 0 | 0 | -0.1 | -0.4 | -0.1 | -0.1 | -0.1 | 0 | -0.2 | -0.3 | -0.5 | -0.1 | 0.9 | -0.4 | 0 | 0 | -0.8 | -1.2 | -0.5 | -0.4 | -0.1 | -0.1 | -0.1 | -0.3 | -0.9 | -0.8 | -0.3 | -0.8 | -0.5 | 0 | -0.2 | -0.4 | -0.7 | -0.4 | -0.3 | -0.4 | -0.1 | 0 | -0.3 | -0.3 | 0 | 0 | -0.2 | -0.1 | -0.1 | -0.1 | -0.2 | 0 | 0.1 | -0.2 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0 | 0.2 | -0.8 | -0.1 | 0.6 | -0.1 | -0.4 | 0 | 0.1 | 0 | 1 | -0.6 | At1g02500 | 260913_at | SAM1 | S-adenosylmethionine synthetase gene sam-1 | 10 | ethylene biosynthesis | methionine and S-adenosylmethionine synthesis | methionine degradation I | Methionine metabolism | Selenoamino acid metabolism | Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate | 1.26 | 2.31 | |||||||||||||||||||||||||
At5g47730 | 0.544 | SEC14 cytosolic factor, putative; similar to polyphosphoinositide binding protein SEC14 homolog Ssh1p (Glycine max) | 1.7 | 0 | -0.1 | 0 | 0.9 | 1.5 | 0 | 0.1 | 1 | 0.3 | 0.8 | -0.7 | 0.7 | 0.9 | 1.3 | 0.7 | 0.5 | -0.4 | 0.3 | 1.4 | 0.4 | 0.2 | 0.3 | 0.3 | 0.4 | 0.4 | -0.1 | -0.5 | 0.2 | 0.4 | 0.7 | 0 | 0 | -0.1 | 0.1 | -0.4 | -0.2 | -0.3 | 0 | -0.1 | 0.2 | 0 | 0 | 0.9 | 1.5 | -0.2 | 0.3 | 2.1 | 0.2 | 0.1 | -0.1 | -0.5 | 0.3 | -0.1 | 0.2 | 1.2 | 1.6 | 0.9 | 1.8 | 1.3 | 0.2 | -0.2 | 0.3 | -0.1 | 0.2 | 0.5 | 0.1 | 0 | -0.3 | -0.2 | -0.2 | 0 | 0.2 | -0.2 | 0 | 0 | 0.1 | 1.5 | -0.2 | 0 | 0 | -0.7 | 0.2 | 0.4 | -0.1 | 0 | 0 | -0.1 | -0.2 | -0.4 | -0.1 | -0.3 | -0.3 | -0.5 | -0.4 | -0.6 | 0 | 0.1 | -0.2 | 0 | -0.2 | 0 | 0 | -0.2 | 0.4 | 0 | 0.6 | 0.8 | -0.3 | -0.3 | -0.7 | -0.3 | -0.5 | 0 | -0.1 | -0.1 | 0.2 | 0.2 | 0.3 | 0.3 | -0.4 | 0.2 | 0.6 | 0.5 | -0.1 | -0.2 | -0.1 | -0.6 | 0.2 | 0 | -0.2 | -0.5 | -0.2 | -0.5 | -0.4 | 0.4 | 0.5 | -0.4 | -0.1 | -0.3 | -0.1 | 1.2 | -0.3 | -0.3 | -0.3 | 0.2 | 0.1 | 0 | -0.6 | -1.4 | -1.2 | -0.5 | -0.1 | -0.3 | -0.4 | -1.2 | -0.6 | -0.4 | 0 | 0.3 | 0 | 0 | -0.6 | -0.6 | -0.1 | -0.2 | 0 | -0.1 | -0.2 | -0.4 | -0.1 | -1.3 | -0.2 | -0.2 | -0.1 | 0 | -0.4 | -0.7 | -0.9 | -1.2 | -0.7 | -0.9 | -0.4 | -0.5 | -0.2 | -0.3 | 0 | -0.2 | -0.1 | -0.5 | -0.1 | -0.3 | -0.3 | 0 | 2.7 | 1.8 | -0.4 | -0.7 | 0 | 0 | -0.2 | 0.2 | 0 | -0.5 | 0.8 | -1.4 | -1.8 | 0.5 | -0.3 | -0.2 | -0.3 | -0.5 | -0.1 | 0.3 | -0.6 | At5g47730 | 248769_at | SEC14 cytosolic factor, putative; similar to polyphosphoinositide binding protein SEC14 homolog Ssh1p (Glycine max) | 4 | Miscellaneous acyl lipid metabolism | 2.10 | 4.55 | ||||||||||||||||||||||||||||||
At1g74000 | 0.543 | SS3 | encodes a protein similar to strictosidine synthase, which is involved in the production of monoterpene indole alkaloids. This gene belongs to a family of 13 members in Arabidopsis. | 2.4 | -0.2 | -0.2 | -0.2 | 0.3 | 0.8 | 0.7 | 0.7 | 0.8 | 1 | 2.3 | -0.1 | 2.3 | 2.1 | 1.4 | 3 | 1.5 | 0.2 | -0.2 | 2.6 | 1.3 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1 | 0.1 | 0.5 | 0.1 | 1.2 | 2.3 | 1 | 2.2 | 0.9 | 2.5 | -0.5 | 0.9 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.3 | 0.4 | 0.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.4 | 0.3 | -0.2 | -0.2 | -0.2 | 0.8 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.3 | -0.2 | -0.2 | -0.2 | 0.7 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.6 | -0.2 | -0.2 | 0.9 | 2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.5 | 1.6 | 2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.8 | -0.2 | 1.6 | 0.5 | -0.2 | 0.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.5 | -0.2 | 0.6 | 0.9 | -0.2 | 0.8 | -0.2 | -0.2 | -0.6 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1.2 | -1.2 | -1.2 | -1.7 | -0.1 | 0.1 | -0.4 | -0.1 | -0.2 | -0.2 | 0.3 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1 | -0.2 | -0.3 | -0.6 | -0.2 | At1g74000 | 260335_at | SS3 | encodes a protein similar to strictosidine synthase, which is involved in the production of monoterpene indole alkaloids. This gene belongs to a family of 13 members in Arabidopsis. | 4 | Terpenoid biosynthesis | Indole and ipecac alkaloid biosynthesis | 2.07 | 4.80 | ||||||||||||||||||||||||||||
At1g30000 | 0.542 | glycoside hydrolase family 47 protei | 0.4 | -0.1 | -0.1 | 0 | 0.4 | 0.3 | 0.4 | 0.3 | 0.3 | 0.3 | 0.5 | -0.1 | 0.3 | 0.3 | 0 | 0.2 | 0.5 | 0 | 0.4 | 0.5 | 0.4 | 0.3 | 0.4 | 0.2 | 0.2 | 0 | 0 | 0.1 | 0 | 0.2 | 0.3 | 0 | 0.1 | -0.1 | 0 | -0.1 | 0 | -0.2 | 0 | 0.1 | 0 | 0.2 | 0.3 | 0 | 0.3 | -0.1 | 0.5 | 0.2 | 0 | 0 | 0 | -0.1 | 0.1 | 0 | 0.1 | 0.2 | 0.7 | 0 | 0.8 | 0.3 | 0.5 | -0.1 | 0 | 0 | 0 | 0.1 | 0.3 | 0.1 | -0.1 | 0.5 | -0.2 | -0.2 | -0.1 | 0 | -0.3 | -0.2 | -0.1 | 0 | -0.1 | -0.2 | -0.2 | -0.3 | 0 | 0 | -0.3 | -0.2 | 0.1 | 0 | 0 | -0.1 | -0.1 | -0.1 | -0.2 | -0.3 | -0.1 | 0.1 | -0.4 | -0.1 | 0 | -0.2 | 0 | 0 | -0.2 | 0 | 0.2 | 0 | 0.1 | 0.5 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | 0 | -0.1 | 0 | 0.1 | 0.3 | 0 | 0.1 | 0 | -0.2 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | -0.1 | 0 | 0 | 0 | 0.3 | 0 | -0.3 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.1 | -0.4 | -0.1 | 0 | -0.1 | -0.2 | 0.2 | -0.2 | -0.1 | 0.2 | 0 | 0.1 | -0.2 | 0.1 | -0.6 | -0.1 | -0.1 | -0.4 | -0.6 | -0.4 | -0.6 | -0.3 | -0.3 | 0.1 | -0.3 | -0.3 | -0.4 | -0.5 | -0.1 | -0.2 | -0.2 | -0.4 | -0.2 | -0.4 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | -0.2 | 0 | 0.1 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0.8 | 0.5 | 0.1 | 0.4 | 0.1 | -0.1 | 0 | 0.2 | 0 | -0.3 | 0.5 | -0.5 | -0.6 | -0.5 | 0 | -0.2 | -0.1 | 0 | 0 | 0.8 | -1 | At1g30000 | 260029_at | glycoside hydrolase family 47 protei | 2 | Glycan Biosynthesis and Metabolism | N-Glycan biosynthesis | Glycan Biosynthesis and Metabolism | High-mannose type N-glycan biosynthesis | 0.96 | 1.90 | ||||||||||||||||||||||||||||||
At2g17720 | 0.537 | oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to prolyl 4-hydroxylase, alpha subunit, from Gallus gallus, Rattus norvegicus, Mus musculus | 0.7 | -0.1 | -0.1 | -0.5 | 0.3 | 0.6 | 0.6 | 0.5 | 1.3 | 0.9 | 1 | 0.1 | 0.8 | 0.9 | 0.1 | 1.2 | 0.9 | 0.6 | 1 | 0.9 | 0.8 | 1.2 | 0.2 | 0.2 | 0.5 | 0.4 | 0.1 | 0 | 0.1 | 0.4 | 0.6 | 0 | 0.8 | 0 | 0 | -0.4 | -0.2 | -0.4 | -0.1 | -0.2 | 0.2 | 0.5 | 0.8 | 0.9 | 1.4 | 0 | 1.1 | 1.7 | 1.2 | 0.8 | -0.2 | -0.2 | 0.1 | 0 | 0.6 | 0.6 | 1.3 | 0.4 | 1.2 | 0.6 | 1.3 | 0 | 0.4 | 0.2 | 0.1 | 0.6 | 0.5 | 0.3 | 0.3 | 0.3 | -0.3 | -0.1 | -0.2 | -0.2 | -0.4 | -0.3 | -0.2 | 0.8 | -0.1 | 0 | -0.3 | -0.5 | -0.2 | 0.3 | -0.4 | -0.2 | -0.2 | -0.4 | -0.2 | -0.4 | -0.2 | -0.2 | -0.6 | -0.5 | 0 | 0.3 | -0.4 | -0.3 | 0 | -0.4 | 0 | 0 | 0.2 | 0.1 | 0.7 | -0.1 | 0 | 0.4 | -0.3 | -0.2 | -0.5 | -0.8 | -0.7 | -0.6 | -0.7 | -0.3 | -0.7 | 0 | -0.1 | 0.5 | -0.3 | -0.2 | -0.2 | -0.2 | -0.3 | -0.1 | -0.1 | -0.3 | -0.1 | -0.3 | -0.2 | -0.3 | 0.1 | -0.1 | -0.4 | -0.3 | -0.4 | -0.3 | -0.4 | -0.1 | -0.1 | 0 | -0.6 | -0.1 | -0.4 | -0.6 | -0.6 | -0.2 | -0.6 | -0.8 | -0.2 | -0.3 | -0.3 | -0.2 | -0.4 | -0.2 | -0.1 | -0.2 | -0.3 | -0.2 | -0.5 | -0.3 | -0.3 | -1.3 | -1.4 | -0.3 | -0.6 | -0.4 | -0.6 | -0.4 | -0.3 | -0.9 | -1.3 | -0.4 | -1 | -0.4 | -0.4 | -0.4 | -0.5 | -0.5 | -0.3 | -0.2 | -0.6 | -0.3 | -0.2 | -0.2 | -0.2 | -0.1 | -0.1 | -0.2 | -0.1 | 0.2 | 0.2 | 0.2 | 1.3 | 1.7 | 0.9 | 0.8 | 0.4 | -0.3 | -0.4 | 0.3 | 1 | -0.1 | 1.7 | -0.9 | -0.1 | -0.9 | -0.4 | 0 | -0.1 | 0.1 | 0 | 1 | -2.1 | At2g17720 | 264592_at | oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to prolyl 4-hydroxylase, alpha subunit, from Gallus gallus, Rattus norvegicus, Mus musculus | 2 | Biosynthesis of Amino Acids and Derivatives | Prolin/Hydroxyproline from glutamate | 1.93 | 3.91 | ||||||||||||||||||||||||||||||
At3g06300 | 0.537 | Encodes a prolyl-4 hydroxylase that can hydroxylate poly(L-proline)and other proline rich peptides, including those with sequences corresponding to those in arabinogalactan proteins and extensins. | 0 | -0.1 | 0 | -0.3 | 0.7 | 0.9 | 0.8 | 0.9 | 0.4 | 1.4 | 0.8 | -0.3 | -0.5 | 0.5 | 0 | 0.4 | 0.6 | 0.9 | 1.2 | 0.5 | 1.1 | 0.9 | 0.1 | 0.3 | 0.3 | 0.1 | 0 | 0.1 | 0.1 | 0.3 | 0.4 | 0 | 0.4 | 0 | -0.3 | 0 | -0.3 | 0 | 0 | 0 | 0.5 | 0.5 | 0.7 | 0.6 | 0.7 | -0.2 | 0.4 | 2 | 0.8 | 1.4 | -0.1 | 0 | 0.2 | 0.2 | 0.7 | 1.1 | 1.5 | 0.6 | 1.7 | 0.8 | 1.4 | 0.2 | 0.4 | -0.1 | 0 | -0.1 | 0.2 | 0 | 0.2 | 0.3 | 0.1 | -0.1 | 0 | 0.1 | -0.1 | 0 | -0.1 | 0.5 | 0 | -0.3 | 0.2 | 0.1 | 0.3 | 0.4 | -0.2 | 0 | 0 | -0.1 | -0.4 | -0.3 | 0 | 0 | 0 | 0 | 0.4 | 0.5 | -0.3 | -0.2 | -0.1 | -0.2 | -0.2 | 0 | -0.1 | -0.2 | 0.3 | -0.7 | -0.5 | -0.4 | -0.3 | -0.5 | -0.4 | -1 | -1 | -0.7 | -0.2 | -0.2 | -0.5 | -0.5 | -0.4 | -0.5 | -0.4 | -0.4 | -1.4 | -1.8 | -1.2 | -0.8 | 0 | 0.1 | -0.2 | -0.5 | 0.1 | 0 | 0.3 | 0.3 | -0.1 | -0.2 | -0.3 | -0.1 | -0.3 | -0.2 | 0 | 0.2 | 0 | -0.2 | -0.8 | -0.5 | -0.1 | -0.4 | -0.6 | -0.4 | -0.2 | -0.2 | -0.3 | 0 | -0.4 | -0.2 | -0.4 | -0.1 | -1 | 0.2 | -0.4 | 0.1 | -0.1 | 0.1 | -0.2 | 0.2 | -0.2 | -0.1 | -0.5 | -0.4 | -0.3 | -0.4 | -0.6 | -0.3 | -1 | -0.6 | -0.2 | -0.5 | -0.6 | -0.2 | -0.2 | 0 | -0.5 | 0.1 | 0 | -0.4 | -0.2 | 0 | -0.3 | -0.3 | 0.1 | -0.1 | -0.2 | -0.3 | 0.6 | 0.3 | 0.4 | 0.6 | 0.6 | 0.3 | -0.3 | 0.2 | 0.2 | 0.3 | 1.8 | -1.2 | -0.2 | -0.9 | -0.6 | 0 | -0.1 | 0 | 0.3 | -0.8 | -0.6 | At3g06300 | 258852_at | Encodes a prolyl-4 hydroxylase that can hydroxylate poly(L-proline)and other proline rich peptides, including those with sequences corresponding to those in arabinogalactan proteins and extensins. | 6 | procollagen-proline 4-dioxygenase activity | peptidyl-proline hydroxylation to 4-hydroxy-L-proline | Biosynthesis of Amino Acids and Derivatives | Prolin/Hydroxyproline from glutamate | 1.77 | 3.86 | |||||||||||||||||||||||||||||
At1g74010 | 0.528 | strictosidine synthase family protein | 2.7 | -0.6 | -0.6 | -0.6 | 0.4 | 0 | 0.2 | 0.4 | 0.9 | 1 | 2.8 | 0.7 | 4.5 | 1.9 | 0.4 | 5.5 | 1.5 | 0.5 | 2.2 | 2.8 | 1.9 | 4.6 | 0.9 | -0.6 | -1.5 | 2 | -0.5 | -0.6 | -0.6 | -1.5 | -0.6 | 1 | -0.6 | -0.3 | -2.7 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 3.4 | 3.4 | -0.6 | -0.6 | 0.1 | 2 | 1.8 | -0.6 | -1.2 | -0.1 | 0.2 | 0.3 | 0.6 | 2.1 | 0.3 | 2.2 | 0.8 | 2.3 | -0.4 | 0.5 | -0.6 | -0.6 | -0.6 | 1.3 | -0.6 | -0.6 | -0.6 | -1.4 | 0.3 | 0.7 | -0.9 | -0.2 | -1.8 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 0.2 | 1.2 | -1.3 | 0.5 | -0.3 | 0 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.1 | 1 | -1.1 | 0.8 | -0.4 | 0 | -0.6 | -0.6 | -0.6 | -0.6 | 0.1 | 1.1 | -0.5 | 1 | -0.6 | 1.9 | 0.8 | 1.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.4 | 1.1 | 0 | 2.1 | 1.5 | 1.5 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.8 | 0 | 1.3 | -0.5 | 2.3 | -0.1 | -0.4 | 3.2 | 2.5 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 0.2 | -0.1 | 0.3 | -0.1 | -0.1 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.8 | -0.4 | -0.6 | -2.4 | 0.3 | 1 | -0.1 | -0.7 | -0.8 | -1 | -1.8 | -0.4 | 0.4 | 0.6 | -0.7 | -0.8 | -1.6 | 0 | 1.1 | -1.5 | 0.6 | -0.5 | -1.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 1.4 | 0.2 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 0.9 | 1.1 | -0.4 | -2.4 | 0.1 | At1g74010 | 260386_at | strictosidine synthase family protein | 2 | Terpenoid biosynthesis | Indole and ipecac alkaloid biosynthesis | 3.80 | 8.34 | ||||||||||||||||||||||||||||||
At3g46690 | 0.527 | UDP-glucoronosyl/UDP-glucosyl transferase family protein | -0.2 | -0.8 | -0.2 | -0.2 | 1.3 | 2.4 | 1.9 | 2.2 | 2.5 | 2.8 | 1.3 | 1.1 | -0.2 | 1.3 | 0.5 | 1.6 | -0.2 | 2.5 | 2 | -0.2 | 3.6 | 2.5 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.6 | 3 | -0.2 | 2.2 | -0.2 | 2.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.4 | 0 | -0.6 | -0.5 | -0.2 | 0.3 | 0.6 | 0.7 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0 | -0.4 | 0 | 0 | 0.1 | 0.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.4 | -0.4 | -0.2 | -0.3 | 0 | -0.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1 | -1 | -0.2 | -0.3 | 0.8 | 0.8 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.5 | -0.3 | 0.4 | 0.1 | 0.4 | 0.8 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.4 | -0.7 | -1.3 | 0 | -0.2 | 0 | 0 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -1 | -0.4 | -0.4 | -0.2 | -0.1 | 0.5 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.3 | -0.9 | -2 | -0.5 | 0.5 | -0.2 | 0.2 | 0 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.1 | -0.1 | -0.2 | 0.3 | -0.2 | -0.2 | 0.3 | -0.2 | -0.2 | -0.2 | 1.3 | 0.3 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.4 | -0.2 | -0.2 | -0.2 | -0.2 | At3g46690 | 252484_at | UDP-glucoronosyl/UDP-glucosyl transferase family protein | 1 | Glycosyl transferase, Family 1 | 2.55 | 5.68 | ||||||||||||||||||||||||||||||
At5g48410 | 0.524 | ATGLR1.3 | plant glutamate receptor family, member of Putative ligand-gated ion channel subunit family | -0.2 | -0.6 | -0.5 | -0.6 | 0.7 | 1.9 | 1.2 | 1 | 1.2 | 1.2 | 0.6 | -0.7 | 1.3 | 1.4 | 0.9 | 2 | 0.1 | -0.3 | 0.8 | 1 | 1.4 | 1.8 | 0.5 | 0 | 0.6 | 0.5 | -0.4 | -0.2 | 0 | 0.1 | 0.4 | 0.5 | 0 | -0.4 | 0 | -0.7 | -0.3 | -0.3 | -0.4 | 0 | -0.4 | -0.3 | -0.1 | 1.5 | 2.4 | 0.1 | 0 | -0.2 | 0.4 | 0.4 | -0.2 | -0.3 | -0.3 | -0.3 | -0.4 | -0.2 | 1.8 | -0.1 | 1.9 | -0.2 | 0.7 | -0.4 | 0 | -0.2 | 0.2 | 0.1 | -0.2 | -0.3 | 0.4 | -0.4 | -0.6 | -0.4 | 0.3 | -0.4 | -0.2 | -0.4 | 0 | 0.3 | 0.2 | 0 | -0.2 | -0.3 | 0 | -0.4 | -0.3 | 0.2 | -0.1 | -0.4 | -0.3 | 0.3 | 0.2 | -0.4 | -0.5 | -0.6 | 0.2 | -0.3 | -0.4 | 0.3 | 0.1 | 0.1 | 0 | 0.2 | 0.4 | 0 | -0.6 | -0.5 | 1.1 | 0.6 | -0.5 | 0.3 | -0.1 | 0.2 | 0 | 0.3 | 0.2 | 0 | -0.2 | -0.1 | 0 | -0.3 | -0.6 | 0.4 | 0.1 | 0 | 0 | 0.1 | 0 | -0.3 | -0.1 | -0.2 | -0.4 | -0.6 | 0 | -0.3 | -0.8 | -0.6 | -0.2 | -0.4 | -0.2 | -0.2 | -0.1 | 0.2 | 0.5 | -0.4 | 0 | 0.2 | 0 | -0.2 | -0.3 | 0.2 | -0.1 | -0.6 | 0.1 | -0.3 | 0 | 0.5 | 1.9 | -0.2 | 0.7 | 0 | -0.5 | 0.3 | -0.2 | -0.8 | -0.2 | -0.4 | 0.3 | -0.8 | -0.2 | -0.4 | -0.2 | -0.4 | -0.2 | -0.5 | -0.3 | 0 | -0.5 | -0.7 | -1 | -1.3 | -0.7 | -0.6 | -0.6 | -0.7 | -0.2 | 0 | 0.2 | -0.3 | -0.1 | -0.6 | 0.3 | -0.3 | 0 | 0 | 0 | 0 | 0 | -0.7 | -0.3 | -0.3 | -0.6 | 0.5 | 0.1 | -0.8 | 0.6 | -0.4 | 0.7 | -1.3 | 0.2 | 0 | 0.1 | -0.4 | -0.2 | 1 | -0.7 | At5g48410 | 248701_at | ATGLR1.3 | plant glutamate receptor family, member of Putative ligand-gated ion channel subunit family | 2 | calcium ion homeostasis | response to light | Ligand-Receptor Interaction | Ion channels | 1.99 | 3.74 | |||||||||||||||||||||||||||
At5g44240 | 0.518 | haloacid dehalogenase-like hydrolase family protein | -0.2 | -0.1 | -0.2 | -0.2 | 0.3 | 0.6 | 0.5 | 0.4 | 0.5 | 0.7 | 0.8 | 0 | 0.8 | 0.6 | 0.3 | 0.5 | 0.7 | 0.3 | 0.1 | 0.7 | 0.7 | 0.3 | 0 | 0.2 | 0.3 | 0.3 | 0 | 0.1 | 0 | 0.3 | 0.5 | 0 | 0.3 | -0.1 | 0.5 | -0.1 | 0 | -0.1 | 0 | 0.1 | 0 | 0.1 | 0.2 | 0.5 | 1.3 | 0.1 | 0.4 | 1.1 | 0.4 | 0.3 | 0 | -0.1 | 0 | 0.1 | 0.2 | 0 | 1.3 | -0.1 | 1.6 | 0 | 0.7 | -0.1 | 0.3 | -0.2 | -0.3 | 0 | 0.1 | 0.2 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0.2 | -0.3 | -0.1 | -0.3 | 0 | -0.3 | -0.3 | -0.1 | 0 | 0 | -0.2 | 0 | 0 | -0.2 | -0.1 | -0.2 | 0 | -0.1 | 0 | -0.1 | 0 | 0.1 | 0 | 0 | 0.3 | -0.1 | 0 | 0 | 0.1 | 0.3 | 0.3 | -0.1 | -0.1 | -0.1 | 0 | 0 | 0.2 | -0.1 | 0 | -0.1 | 0.2 | -0.3 | 0 | -0.3 | -0.1 | -0.4 | -0.6 | -0.1 | 0 | 0 | 0 | -0.2 | -0.1 | -0.1 | 0 | -0.1 | 0.1 | -0.3 | -0.2 | -0.3 | -0.1 | 0.1 | -0.1 | 0 | 0.1 | 0.3 | -0.3 | -0.3 | -0.2 | -0.3 | -0.4 | -0.3 | -0.3 | -0.4 | -0.1 | -0.1 | 0 | -0.1 | -0.2 | -0.3 | 0.1 | -0.7 | 0 | -0.3 | -0.1 | -0.5 | -0.8 | -0.4 | 0 | -0.2 | -0.5 | -0.3 | -0.1 | -0.1 | -0.3 | -0.1 | 0.4 | -0.1 | -0.1 | -0.7 | -0.9 | -1 | -0.7 | -0.3 | -0.2 | 0 | 0 | 0 | -0.3 | -0.1 | 0.1 | 0.1 | 0 | 0.1 | -0.1 | -0.2 | -0.3 | 0.1 | 0.7 | -0.2 | 0 | 0 | 0 | -0.1 | 0.2 | 0.3 | 0.1 | 0.2 | -0.4 | -0.7 | -0.1 | 0 | -0.4 | -0.2 | 0.4 | 0 | 1 | -1.4 | At5g44240 | 249089_at | haloacid dehalogenase-like hydrolase family protein | 2 | Miscellaneous acyl lipid metabolism | 1.21 | 3.03 | ||||||||||||||||||||||||||||||
At1g79530 | 0.515 | similar to glyceraldehyde-3-phosphate dehydrogenase from Pinus sylvestris | 2.2 | -0.1 | 0 | -0.1 | 0 | 0.7 | 0.3 | 0.2 | 0.9 | 0.7 | 0.1 | 0.2 | 1.5 | 0.7 | 1 | 1.9 | -0.2 | 0 | 1.6 | 0.2 | 0.6 | 1.7 | -0.4 | 0.1 | 0 | -0.2 | -0.1 | -0.1 | 0 | 0 | -0.6 | -0.1 | -0.1 | 0 | 0.3 | -0.7 | -0.6 | -0.3 | -0.7 | 0 | -0.5 | 0.4 | 0.5 | 0.6 | 1.2 | -1.2 | -0.1 | 1.5 | 0.9 | 0.9 | -0.1 | -0.3 | -0.2 | -0.1 | -0.5 | -0.5 | 0.5 | 0.7 | 0.8 | 0.5 | 0 | -0.3 | -0.2 | 0.2 | -0.1 | -0.1 | 0.2 | -0.2 | -0.2 | -0.5 | -0.1 | -0.2 | -0.3 | -0.4 | -0.4 | -0.2 | -0.1 | -0.1 | 0 | 0.1 | 0.3 | 0.4 | 0.4 | 0.5 | 0 | 0 | -0.2 | -0.4 | -0.2 | -0.3 | 0 | 0.4 | 0.5 | -0.2 | 0.2 | 0 | -0.4 | -0.2 | -0.4 | -0.5 | -0.5 | -0.6 | -0.3 | 0.3 | 0.9 | 0.5 | 1.3 | 0.2 | -0.1 | 0 | 0 | -0.2 | -0.6 | -0.3 | -0.1 | -0.2 | 0.5 | 0 | 0.6 | 0.6 | 0 | 0 | -0.4 | -0.7 | -0.8 | -0.3 | -1 | 0 | 0.5 | 0.4 | 1 | -0.3 | 0.2 | -0.4 | 0 | 0 | 0 | -0.1 | -0.2 | 0 | 0 | -0.3 | -1.1 | 0.5 | 0.7 | 0 | -0.1 | 0.2 | 0.4 | 0 | 0.2 | -0.1 | -0.2 | -0.8 | -0.4 | -0.3 | -0.3 | -0.9 | -0.3 | 0.1 | 0 | -0.1 | -0.1 | -0.3 | -0.2 | -0.2 | 0 | -0.4 | 0 | -0.1 | 0 | -0.4 | -0.5 | -0.6 | -0.2 | 0 | 0 | 0 | 0 | -0.5 | -0.5 | 0 | -0.3 | -0.1 | -0.4 | -0.3 | -0.2 | -0.1 | -0.3 | -0.2 | -0.5 | 0.1 | -0.3 | -0.1 | 0.5 | 0.4 | 0.7 | -0.4 | -0.6 | -1.8 | -0.2 | 0.3 | -0.1 | 0.9 | 2 | -1.8 | 0.2 | -1.9 | -0.4 | -0.3 | 0 | 0.1 | 0 | 1.2 | 0.3 | At1g79530 | 262939_s_at | similar to glyceraldehyde-3-phosphate dehydrogenase from Pinus sylvestris | 4 | C-compound and carbohydrate metabolism | glycolysis and gluconeogenesis | gluconeogenesis | glycerol degradation II | sorbitol fermentation | fructose degradation (anaerobic) | acetate fermentation | glycolysis I | glyceraldehyde 3-phosphate degradation | glycolysis IV | Glycolysis / Gluconeogenesis | Intermediary Carbon Metabolism | 1.77 | 4.23 | |||||||||||||||||||||||||||
At3g29200 | 0.515 | CM1 | chorismate mutase, chloroplast | 0 | -0.1 | 0 | 0.8 | 0.2 | 0.6 | -0.3 | -0.1 | 0.3 | 0.2 | 1 | -0.2 | 0.6 | 0.8 | 0.2 | 0.3 | 0.5 | 0 | 0 | 1 | 0.7 | 0.2 | -0.2 | -0.3 | -0.8 | -0.4 | -0.3 | -0.1 | -0.1 | -0.5 | -0.6 | 0 | 0.1 | -0.2 | -0.5 | 0 | -0.4 | -0.2 | -0.3 | -0.1 | 0 | -0.2 | -0.3 | 0.7 | 0.6 | -0.3 | -1 | 0.1 | 0 | -0.1 | -0.2 | -0.2 | 0 | 0.3 | 0 | 0.8 | 0 | 0.5 | -0.4 | 1.2 | 0.2 | -0.1 | 0 | 0 | -0.8 | -0.8 | -0.3 | -0.2 | 0 | -0.5 | 0.1 | -0.1 | 0 | 0.1 | -0.2 | 0 | -0.1 | -0.2 | -0.1 | 0.1 | 0 | 0.2 | 0.1 | 0.2 | 0 | 0 | 0.1 | -0.2 | 0 | 0 | -0.2 | 0.1 | 0 | 0 | 0 | -0.2 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0 | -0.4 | 0 | 0.5 | 0.4 | 0 | 0 | 0.1 | 0.1 | 0.2 | 0.3 | 0.1 | 0 | -0.6 | 0 | 0 | 0 | -0.1 | -0.2 | -0.3 | -0.9 | -0.1 | -0.2 | 0.1 | 0.5 | 0.1 | 0.1 | -0.1 | -0.1 | -0.1 | -0.4 | 0.1 | -0.1 | 0.6 | 0.1 | 0 | 0 | 0 | 0.2 | -0.3 | 0.6 | 0.6 | 0.4 | 0.5 | 0.8 | 1 | -0.4 | -1.5 | 0 | 0 | 0.2 | -0.1 | 0 | 0.6 | -1.9 | -1.5 | -0.4 | 0.1 | 0 | 0 | 0 | 0 | 0.5 | 0.4 | 0.3 | 0.1 | -0.1 | -0.3 | 0 | 0.2 | 0 | 0.3 | 0 | 0.2 | 0 | -0.1 | -0.4 | -0.2 | 0 | -0.3 | -0.1 | 0.2 | 0.3 | 1.3 | 0.6 | -0.1 | 0 | 0 | 0 | 0.3 | 0.8 | 0.3 | 0 | -0.1 | 0 | -0.4 | -0.3 | -0.1 | 0 | 0.2 | 0.3 | 0.5 | -1.2 | -0.4 | -0.1 | -0.5 | -0.1 | 0 | 0.6 | -0.3 | -1 | 0 | At3g29200 | 257746_at | CM1 | chorismate mutase, chloroplast | 10 | chorismate mutase activity | aromatic amino acid family biosynthesis, shikimate pathway | phenylalanine biosynthesis II | tyrosine biosynthesis I | ascorbate glutathione cycle | Phenylalanine, tyrosine and tryptophan biosynthesis | Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism | Shikimate pathway | chorismate biosynthesis | 1.39 | 3.31 | ||||||||||||||||||||||||
At4g35600 | 0.510 | CONNEXIN 32 | protein kinase family protein, plant-type connexin 32 | 0 | -0.4 | 0 | -0.8 | 0.1 | 0.5 | 0 | -0.2 | 1.5 | 0.2 | 0.7 | 0 | 1.2 | 1 | 0.5 | 1.4 | 0.4 | -0.1 | 0.8 | 0.8 | 1 | 1.3 | -0.1 | 0.1 | 0.3 | 0 | 0 | -0.1 | 0 | 0.2 | 0.6 | 0.2 | 0 | -0.2 | -0.2 | -0.1 | -0.4 | 0 | -0.3 | -0.1 | 0 | 0 | 0.4 | -0.3 | -0.1 | -0.1 | -0.1 | 0.2 | -0.2 | 0 | 1.5 | -0.8 | 0 | -0.1 | 0.6 | 0.8 | 2.1 | 0.5 | 1.3 | 0.8 | 1.8 | -0.5 | 0.4 | 0.7 | 0.4 | 0.2 | 0.6 | 0.5 | 0.1 | 0 | -0.2 | 0.1 | 0 | -0.1 | -0.1 | -0.1 | 0.2 | 1.8 | -0.2 | -0.4 | -0.2 | 0.1 | -0.1 | 0 | 0 | 0 | -0.4 | -0.1 | -0.2 | 0.1 | -0.3 | -0.4 | 0 | -0.2 | 0 | 0 | 0 | 0.1 | 0.4 | 0.2 | 0.2 | 0.3 | -0.4 | -0.2 | 0 | -0.2 | 0.1 | 0 | -0.3 | 0 | -0.1 | -0.5 | -0.2 | -0.2 | -0.6 | -1.4 | -0.2 | -0.2 | 0 | 0 | 0 | 0.1 | 1.2 | 1.4 | 0.6 | 1 | 0.1 | 0 | -0.4 | -0.2 | -0.1 | 0.1 | 0 | -1.2 | -0.7 | -0.1 | 0.2 | -0.5 | -0.4 | -0.3 | -0.5 | 0.6 | 0 | -0.4 | -1 | -0.7 | 0 | 1 | 0.5 | -0.9 | -1.1 | -0.3 | -0.2 | 0.1 | -0.2 | 0 | 0.8 | 0 | -0.2 | -0.9 | -0.2 | -1.3 | -1.4 | -0.2 | -0.4 | 0 | -0.3 | -0.5 | -0.7 | -0.3 | -0.1 | -1.4 | -0.5 | -0.3 | -0.5 | -0.3 | -0.3 | -0.5 | -0.1 | -0.3 | -0.1 | -0.3 | -0.7 | -0.4 | -0.1 | 0.4 | 0.2 | -0.2 | 0 | -0.1 | 0.2 | 0.3 | -0.1 | 0.3 | 1.7 | 1.3 | 0 | 0.3 | 0.5 | -0.2 | 0.2 | -0.1 | -0.5 | 0.1 | -0.2 | -0.2 | -0.3 | -0.5 | -0.5 | -0.1 | -0.5 | -1.4 | 0 | 0.4 | -1.8 | At4g35600 | 253147_at | CONNEXIN 32 | protein kinase family protein, plant-type connexin 32 | 2 | Inositol phosphate metabolism | Nicotinate and nicotinamide metabolism | Benzoate degradation via CoA ligation | 2.14 | 4.00 | ||||||||||||||||||||||||||||
At5g46360 | 0.510 | KCO3 | outward rectifying potassium channel, putative (KCO3), member of KCO-like protein 3 family | 0 | -0.6 | 0.2 | 0 | 0.1 | 0 | 0.3 | 0 | 0.3 | 0.2 | 0.4 | -0.3 | 0.7 | 1 | 0.4 | 0.5 | 0 | -0.3 | 0.9 | 0 | 1.5 | 1.5 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.3 | 0 | -0.5 | 0 | -0.3 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.3 | 0 | 1.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0 | -0.2 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | -0.3 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.2 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.3 | 0.2 | 0.5 | 0.4 | 0.3 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | -0.2 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | -0.7 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | At5g46360 | 248897_at | KCO3 | outward rectifying potassium channel, putative (KCO3), member of KCO-like protein 3 family | 2 | Ligand-Receptor Interaction | Ion channels | 0.65 | 2.34 | ||||||||||||||||||||||||||||
At5g48400 | 0.507 | ATGLR1.2 | plant glutamate receptor family, member of Putative ligand-gated ion channel subunit family | 0.4 | -0.6 | -0.9 | -0.1 | 1.2 | 2 | 1.3 | 1.2 | 2.2 | 1.5 | 1.3 | -0.5 | 1.3 | 1.5 | 1 | 2.2 | 0 | -0.3 | 1.7 | 1.6 | 2.9 | 3 | 0.8 | -0.2 | 0.3 | -0.1 | 0.6 | -0.2 | -0.1 | 0 | -0.2 | 0.3 | -0.1 | -0.5 | -0.4 | -0.8 | -0.6 | -0.6 | -0.3 | -0.5 | -0.2 | -0.5 | 0.1 | 1 | 1.8 | 0 | 0.4 | -0.2 | 0 | 0.4 | -0.4 | -0.7 | -0.1 | -0.5 | -0.4 | -0.5 | 3.4 | -0.4 | 3.6 | -0.3 | 2.5 | -0.6 | 0.3 | -0.8 | -0.4 | -0.3 | -0.3 | -0.5 | -0.1 | 0 | -0.4 | -0.3 | 0.1 | -0.1 | -0.1 | -0.4 | 0.1 | 0.5 | -0.3 | -0.4 | -0.4 | -0.6 | -0.6 | -0.7 | -0.3 | -0.2 | -0.2 | -0.5 | -0.4 | 0.2 | -0.7 | -0.9 | -0.3 | -0.6 | -1 | -0.1 | -0.5 | -0.1 | 0.8 | 0.5 | 0.7 | 0.3 | -0.3 | -0.4 | -0.6 | -0.5 | -0.3 | 0.5 | 0.2 | 0.2 | 0.4 | 0.3 | 0.6 | 0.6 | -0.3 | -0.4 | -0.3 | -0.7 | -0.6 | -0.3 | -0.2 | 0.3 | 0.9 | 1.1 | 1 | 1.2 | -0.3 | -0.8 | -0.3 | -1.1 | -0.2 | -0.9 | -0.6 | -0.1 | -0.8 | -0.3 | 0.1 | -0.4 | 0 | -0.1 | -0.4 | 0.7 | 0 | 0 | 0 | -0.6 | -0.3 | -0.4 | -0.6 | -0.4 | -0.2 | -0.4 | -0.3 | -0.2 | -0.2 | 1.8 | 3.2 | -0.1 | 0.1 | 0.5 | -0.8 | -0.3 | -0.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.2 | -0.4 | 0 | 0 | -0.1 | -0.3 | -0.7 | 0 | -0.2 | -0.6 | -0.6 | -0.5 | -0.5 | -0.5 | -0.3 | -0.6 | -0.5 | -0.5 | 0.4 | 0 | 0.3 | 0 | -0.6 | 0.5 | -0.7 | -0.3 | -0.5 | 0.2 | -0.3 | -0.9 | -0.5 | -0.5 | -0.9 | -0.3 | 0.3 | 0.7 | -1.4 | 0 | -0.3 | -0.2 | -0.3 | 0.4 | -0.4 | 0 | -0.7 | -0.3 | 1.4 | -1.1 | At5g48400 | 248700_at | ATGLR1.2 | plant glutamate receptor family, member of Putative ligand-gated ion channel subunit family | 2 | calcium ion homeostasis | response to light | Ligand-Receptor Interaction | Ion channels | 2.63 | 5.11 | |||||||||||||||||||||||||||
At5g64440 | 0.506 | amidase family protein, low similarity to enantiomerase-selective amidase (Rhodococcus sp.) | 0.6 | -0.1 | 0 | -0.3 | 0 | -0.1 | -0.1 | 0 | 0.1 | 0.5 | 0.4 | 0 | 0.5 | 0.3 | 0 | 0.3 | 0.3 | 0.2 | 0.3 | 0.2 | 0.3 | 0.2 | 0 | -0.1 | 0.1 | 0.2 | -0.2 | 0 | -0.2 | 0 | 0.4 | -0.1 | 0 | 0 | -0.4 | 0 | -0.1 | 0 | 0 | 0.2 | 0 | 0 | 0 | 0.1 | 0.5 | -0.1 | 0.2 | 0.4 | 0.5 | 0.2 | 0 | 0.1 | 0.3 | 0.2 | 0.3 | 0.4 | 0.7 | 0.1 | 0.8 | 0.4 | 0.3 | 0.1 | 0 | -0.1 | -0.2 | 0.1 | 0 | 0 | 0 | 0.4 | -0.1 | 0 | 0.3 | 0 | 0 | -0.4 | -0.1 | 0.2 | -0.2 | 0 | -0.1 | 0 | -0.1 | -0.1 | 0 | 0.2 | -0.1 | 0 | 0 | 0 | -0.2 | -0.1 | -0.2 | 0 | 0.3 | 0.2 | -0.1 | 0.1 | -0.2 | 0.1 | 0 | 0.5 | -0.1 | -0.1 | 0.3 | 0.7 | 0.3 | 0.2 | -0.2 | 0.1 | -0.2 | 0.1 | 0 | 0.1 | -0.1 | 0 | 0 | 0.4 | 0.4 | 0.5 | -0.1 | 0 | -0.5 | -0.5 | -0.2 | 0 | 0 | 0 | 0.1 | -0.2 | 0 | 0.1 | 0.2 | 0.1 | -0.2 | -0.2 | -0.1 | -0.2 | 0.2 | -0.1 | -0.1 | 0 | 0.2 | -0.2 | -0.7 | -0.1 | -0.3 | -0.5 | -0.2 | 0 | -0.1 | -0.2 | 0 | -0.1 | -0.3 | -0.2 | -0.3 | -0.4 | 0 | -0.1 | 0 | -0.1 | -0.2 | -1.3 | -0.7 | 0 | 0 | 0 | 0 | -0.1 | 0.1 | -0.9 | -0.6 | 0 | 0 | 0 | 0 | -0.2 | -0.2 | -0.8 | -0.6 | -0.2 | -0.2 | -0.2 | -0.1 | -0.1 | 0.1 | 0 | 0.1 | -0.1 | 0 | -0.2 | -0.2 | -0.2 | -0.1 | 0.4 | 0.1 | 0.1 | 0 | 0.1 | -0.1 | 0 | 0.6 | -0.1 | 1.4 | -1.7 | -0.6 | 0.8 | 0.1 | 0 | 0 | 0.1 | 0 | -0.6 | -0.2 | At5g64440 | 247262_at | amidase family protein, low similarity to enantiomerase-selective amidase (Rhodococcus sp.) | 10 | Lipid signaling | 1.12 | 3.22 | ||||||||||||||||||||||||||||||
At2g47650 | 0.503 | UXS4 | encodes a protein similar to UDP-glucuronic acid decarboxylase. UDP-glucornic acid decarboxylase produces UDP-xylose, which is a substrate for many cell wall carbohydrates including hemicellulose and pectin. UDP-xylose is also known to feedback regulate s | 0.1 | -0.2 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0.6 | 0.6 | 0.4 | 0.1 | 0.6 | 0.3 | 0.1 | 0.6 | 0.3 | 0.1 | 0.6 | 0.4 | 0.6 | 0.6 | -0.1 | 0.2 | 0.1 | 0 | 0 | -0.1 | 0 | 0.1 | 0.2 | -0.1 | 0 | -0.1 | 0 | -0.1 | -0.3 | -0.1 | 0 | -0.2 | 0 | 0.1 | 0 | 0.3 | 1 | 0 | 0.5 | 1.1 | 0.4 | 0.3 | 0.2 | -0.1 | 0.2 | 0 | 0.4 | 0.5 | 1 | 0.2 | 0.9 | 0.4 | 0.7 | 0 | 0.2 | 0 | -0.2 | 0.1 | 0 | -0.2 | 0 | -0.2 | 0 | -0.1 | -0.2 | -0.1 | -0.2 | 0.1 | 0 | 0.1 | 0 | 0 | 0.1 | 0.2 | 0.4 | 0.5 | -0.1 | 0 | 0 | -0.1 | 0.1 | -0.2 | -0.1 | 0.2 | 0 | 0 | 0.5 | 0.1 | -0.3 | -0.2 | -0.1 | -0.3 | 0 | -0.1 | -0.1 | 0 | 0.5 | 0.4 | 0.7 | 0.6 | -0.3 | -0.5 | -0.4 | -0.5 | -0.4 | -0.4 | -0.3 | -0.2 | -0.1 | 0.1 | 0.5 | 0.7 | -0.4 | -0.4 | -0.7 | -0.9 | -0.5 | -0.4 | -0.1 | -0.2 | 0.2 | 0 | 0 | 0 | 0.2 | 0 | -0.2 | -0.1 | -0.1 | 0 | -0.1 | 0 | 0 | 0.2 | -0.3 | -0.1 | 0.6 | 0 | -0.5 | -0.5 | -0.2 | 0.2 | 0.7 | -0.2 | -0.1 | -0.2 | -0.2 | 0 | -0.1 | 0 | -0.2 | -0.3 | 0 | 0.2 | 0 | -0.5 | -0.1 | 0.1 | 0 | 0 | 0 | -0.3 | -0.3 | -0.1 | 0 | -0.2 | 0 | -0.1 | -0.4 | -0.6 | -0.8 | -0.3 | 0 | -0.2 | -0.9 | -0.4 | -0.3 | -0.3 | -0.1 | 0.1 | -0.1 | -0.1 | -0.2 | -0.2 | 0 | -0.3 | 0.4 | 0.4 | 0.1 | -0.1 | 0.1 | 0.2 | -0.2 | 0.1 | -0.3 | 0 | 0.3 | -0.6 | -0.6 | -0.5 | -0.7 | -0.1 | 0 | 0.2 | 0.1 | 0.3 | -0.7 | At2g47650 | 251234_s_at | UXS4 | encodes a protein similar to UDP-glucuronic acid decarboxylase. UDP-glucornic acid decarboxylase produces UDP-xylose, which is a substrate for many cell wall carbohydrates including hemicellulose and pectin. UDP-xylose is also known to feedback regulate s | 4 | D-xylose metabolism | Cell Wall Carbohydrate Metabolism | UDP-carbohydrate metabolism | 1.23 | 2.15 | |||||||||||||||||||||||||||
At3g53180 | 0.501 | similar to glutamine synthetase (Bacillus subtilis) | 1 | -1.4 | -0.2 | -0.7 | 0.5 | 0.2 | 0.3 | 0.3 | 0.5 | 1 | 0.6 | 0.2 | 0.5 | 0.2 | 0.4 | 0.7 | 0.5 | 0.5 | 0.3 | 0.6 | 0.4 | 0 | 0 | 0 | 0.1 | 0.1 | -0.1 | 0.3 | 0.1 | 0.1 | 0.2 | 0 | -0.1 | -0.4 | -0.6 | 0.1 | -0.1 | -0.2 | 0 | 0 | -0.2 | 0 | -0.1 | 0.5 | 0.6 | -0.4 | -0.3 | 1.3 | 0.9 | 0.8 | 0.1 | -0.5 | 0.2 | -0.1 | 0.7 | 0.7 | 1.5 | 0.5 | 1.3 | 0.7 | 1.7 | -0.3 | 0.5 | 0 | 0.3 | 1.2 | 0.6 | 0.2 | 0 | 0.3 | -0.5 | -0.1 | 0 | -0.2 | -0.2 | -0.4 | -0.3 | 0.8 | -0.1 | 0.1 | 0 | -0.3 | -0.1 | 0.2 | -0.4 | -0.1 | -0.2 | -0.3 | -0.2 | -0.3 | -0.2 | -0.1 | 0.2 | -0.1 | 0 | 0 | -0.5 | -0.1 | -0.3 | -0.5 | -0.4 | -0.5 | 0.1 | 0.3 | 1.5 | 0.8 | 0.3 | 0.4 | 0 | 0.4 | 0.2 | 0 | 0 | 0 | -0.1 | 0 | 0.6 | 0.2 | 0 | 0 | -0.1 | 0.4 | 0.5 | 0.9 | 0.6 | 0.6 | -0.3 | -0.2 | 0.6 | 0.6 | 0.3 | 0 | 0 | -0.1 | -0.5 | -0.4 | 0.1 | -0.1 | 0 | -0.2 | -0.4 | 0.7 | 0.9 | -0.5 | -1.1 | 0 | -0.2 | -0.3 | -1.1 | -1.1 | -1.3 | -0.2 | 0 | -0.8 | -0.6 | -0.5 | -1 | 0.9 | 0.1 | 0.2 | -0.1 | -0.2 | -0.3 | -1.5 | -0.3 | -0.3 | 0.1 | -0.1 | -0.2 | -0.4 | -0.2 | -0.9 | -0.3 | -0.2 | 0 | -0.1 | -0.2 | -0.4 | -0.4 | -1.1 | -0.9 | -0.5 | -0.5 | -0.1 | -0.3 | -0.6 | -0.2 | -0.3 | -0.2 | -0.3 | -0.3 | -0.1 | 0 | -0.1 | 0.5 | 0.5 | 0.1 | 0 | 0.1 | 0.2 | -0.3 | 0 | 1.1 | -0.3 | -0.3 | -0.6 | -0.4 | 0 | 0.1 | -0.3 | -0.1 | -0.3 | 0 | -1 | -0.7 | At3g53180 | 251973_at | similar to glutamine synthetase (Bacillus subtilis) | 2 | amino acid metabolism | assimilation of ammonia, metabolism of the glutamate group | nitrogen and sulfur metabolism | glutamine biosynthesis I | ammonia assimilation cycle | nitrate assimilation pathway | 1.80 | 3.25 | |||||||||||||||||||||||||||||
At5g24430 | 0.501 | similar to calcium/calmodulin-dependent protein kinase CaMK1 (Nicotiana tabacum) | 0.8 | -0.2 | -0.4 | -1.3 | 0.7 | 0.9 | 0.3 | 0.4 | 1.3 | 1.1 | 1.6 | -0.3 | 1.9 | 1 | 0.5 | 2.1 | 0.8 | 0 | 1.4 | 1.7 | 1.3 | 1.7 | 0 | 0.3 | 0.2 | 0 | -0.3 | 0 | 0.1 | 0.2 | 0 | -0.1 | -0.3 | -0.2 | 0 | -0.1 | -0.2 | -0.3 | -0.2 | -0.1 | -0.3 | -0.5 | 0 | 0.3 | 1.1 | -0.7 | -0.1 | 0.4 | 0 | 0.1 | 0.3 | -0.8 | -0.2 | -0.1 | 0.3 | 0.7 | 2 | 0.5 | 1.3 | 0.6 | 2 | -0.7 | 0.2 | 0.4 | 0.4 | 0.5 | 0 | 0.2 | 0 | 0.4 | -0.1 | -0.4 | -0.3 | -0.3 | -0.1 | 0 | -0.1 | 1.1 | 0.1 | -0.2 | -0.4 | -0.1 | -0.3 | 0 | -0.3 | -0.4 | -0.1 | -0.1 | 0 | -0.1 | 0.1 | -0.2 | -0.6 | 0 | 0.1 | 0.1 | -0.2 | -0.2 | -0.3 | -0.4 | -0.1 | -0.3 | -0.1 | -0.2 | -0.1 | 0 | 0.2 | 0.2 | -0.2 | 0 | -0.2 | -0.4 | 0 | 0 | -0.2 | -0.3 | -0.1 | 0.1 | 0.3 | 0.2 | -0.1 | -0.1 | 0.1 | 0.1 | 0 | 0 | 0 | -0.6 | 0.2 | 0.1 | 0 | 0.1 | 0.2 | -0.1 | -0.3 | 0.2 | 0.5 | -0.1 | -0.2 | 0 | -0.6 | 0.9 | 0.8 | -0.4 | -1 | -0.5 | -0.8 | -0.3 | 0 | -0.9 | -1.6 | -0.7 | -0.5 | -0.6 | -0.4 | -0.1 | -0.9 | 1.3 | 0.4 | 0 | -0.2 | -0.7 | -1 | -0.9 | -0.1 | -0.3 | -0.3 | -0.1 | -0.2 | -0.3 | -0.3 | -0.3 | 0 | -0.3 | -0.1 | -0.5 | 0 | 0 | -0.1 | 0.3 | 0.1 | -0.2 | -0.5 | -0.2 | -0.2 | -0.4 | -0.3 | -0.4 | -0.3 | -0.1 | -0.3 | -0.3 | -0.2 | -0.6 | -0.3 | 0.3 | -0.1 | -0.2 | 0.4 | 0 | 0.1 | 0 | -0.1 | 0.5 | -1.3 | 0.9 | 0 | 0.7 | -0.9 | -0.1 | -0.4 | -0.5 | 0 | 0.5 | -1.8 | At5g24430 | 249730_at | similar to calcium/calmodulin-dependent protein kinase CaMK1 (Nicotiana tabacum) | 9 | N-terminal protein myristoylation | Inositol phosphate metabolism | Nicotinate and nicotinamide metabolism | Benzoate degradation via CoA ligation | 2.16 | 3.97 |