| Co-Expression Analysis of: | CYP74A, AOS (At5g42650) | Institut de Biologie Moléculaire des Plantes |
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| ________________________ | _____________________________________________ | CYPedia Home | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Stress Data Set | save / view heatmap as: | OpenOffice Table | annotation details for co-expressed genes can be found to the right of the heatmap | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| MS Excel table | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| save / view all data as: | Tab delimited table | For further information on the experiments please go to the Genevestigator database using the experiment-ID given in brackets. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| shown are a maximum of 50 genes with r>0.5 (If more co-expressed genes with r>0.5 exist, they can be saved as Tab delimited data only) | magnitude of change [log2(treatment / control)] | 0 | 0.3 | 0.6 | 0.9 | 1.2 | 1.5 | 1.8 | 2.1 | 2.4 | 2.7 | >3 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | |||||||||||||||||||||
| At5g42650 | 1.000 | AOS, CYP74A | allene oxide synthase; encodes a member of the cytochrome p450 CYP74 gene family that functions as an allene oxide synthase. This enzyme catalyses dehydration of the hydroperoxide to an unstable allene oxide in the JA biosynthetic pathway. | -2 | 0 | -0.3 | -0.1 | 0 | -0.2 | -0.6 | -0.6 | 0 | -0.3 | -0.1 | -0.1 | 0 | -0.6 | -0.2 | -0.6 | -0.3 | -0.5 | -0.1 | 0 | -0.9 | -0.9 | -0.2 | -0.3 | -0.4 | -0.5 | -0.8 | 0 | 0 | -0.1 | -0.3 | -0.2 | -0.1 | -0.7 | -0.9 | -0.5 | -0.6 | -0.4 | -0.4 | -0.5 | -0.9 | -1.1 | -0.8 | 0.4 | 0.4 | -0.2 | -0.3 | -0.1 | -0.6 | -0.4 | -0.4 | -0.3 | -0.1 | -0.2 | -0.4 | 0 | -0.2 | -0.2 | -0.2 | -0.1 | 0 | -0.2 | 0 | 0.4 | 1.6 | 2.8 | 1.7 | 0.4 | 0.2 | -0.2 | 0 | 0.1 | 0.5 | 0.1 | 0.7 | 1.4 | 1 | 1.2 | 0 | 0 | 0.5 | 0 | 0.1 | 1 | 0.2 | 0 | -0.4 | 0.4 | 0 | 0 | -0.3 | 0 | 0.4 | 0.2 | 0.4 | 0 | 0.8 | 0.3 | -0.1 | 0.3 | 0 | -0.4 | -0.2 | 0.5 | 1 | 0.5 | -0.4 | 0.4 | 0.8 | 0.6 | -0.8 | -0.2 | -0.1 | 0.1 | 0 | -0.1 | 0 | 0.2 | 0 | 0.2 | 0.5 | 2.6 | 3.3 | 3.7 | 1.3 | 0.7 | 0 | -0.9 | 1.7 | 1.6 | 2.7 | 0.9 | 0.7 | 0.7 | 0 | 2.6 | 2.6 | 0.6 | 0.7 | 0.3 | 0 | 1.6 | -1.5 | 0.4 | 0.1 | -0.4 | -0.2 | 0.1 | -0.1 | -0.5 | -0.5 | -0.4 | -0.1 | 0.6 | 0.9 | -0.2 | -1.1 | 2.1 | 1.6 | 0.8 | -0.8 | -0.3 | -0.3 | -1.3 | -0.7 | -0.4 | -0.2 | -0.4 | -0.8 | -0.8 | -0.5 | -0.7 | -0.1 | -0.4 | -1.3 | -0.7 | -0.2 | -0.2 | -0.2 | -0.4 | -0.4 | -0.2 | -0.2 | -0.2 | -0.4 | 0 | -0.3 | -0.3 | -0.2 | -0.1 | -0.3 | -0.4 | 0.3 | 0.1 | -0.2 | -0.3 | -0.8 | -1.1 | -0.7 | 0.6 | -1.2 | -0.2 | -0.5 | -2.3 | -7 | 4.1 | 1.2 | 0.5 | 0 | -0.1 | -0.3 | 0.2 | 0.1 | -2.7 | -0.2 | At5g42650 | 249208_at | AOS, CYP74A | allene oxide synthase; encodes a member of the cytochrome p450 CYP74 gene family that functions as an allene oxide synthase. This enzyme catalyses dehydration of the hydroperoxide to an unstable allene oxide in the JA biosynthetic pathway. | 10 | hydro-lyase activity | jasmonic acid biosynthesis | allene oxide synthase activity | response to wounding | response to jasmonic acid stimulus | jasmonic acid biosynthesis | lipoxygenase pathway | Lipid signaling | oxylipin pathway | cytochrome P450 family, allene oxid synthase, oxylipin pathway | 2.73 | 11.26 | ||||||||||||||||||||||||
| At3g25760 | 0.810 | AOC1 | encodes allene oxide cyclase. One of four genes in Arabidopsis that encode this enzyme, which catalyzes an essential step in jasmonic acid biosynthesis. Gene expression is induced during scenescence, a process that involves jasmonic acid signalling pathw | -5.4 | 0 | -0.1 | -0.1 | 0 | 0 | -0.3 | -0.2 | 0.3 | -0.2 | -0.1 | -0.2 | 0 | -0.4 | 0 | -0.3 | -0.2 | -0.2 | 0 | 0 | -0.4 | -0.7 | -0.1 | 0 | 0.2 | -0.3 | -0.4 | 0 | 0 | 0.3 | -0.2 | -0.2 | 0 | -0.4 | -0.5 | -0.3 | -0.3 | -0.2 | 0 | -0.3 | -0.4 | -0.5 | -0.7 | 0.8 | 0.6 | 0 | -0.1 | 0.7 | 0 | 0.4 | -0.3 | -0.2 | 0 | 0 | -0.2 | 0 | 0 | 0 | -0.2 | 0 | 0 | -0.2 | 0 | -0.1 | 1.5 | 2.7 | 1.5 | 0.9 | 0.6 | 0.8 | -0.4 | 0.8 | 0.7 | -0.4 | 1.9 | -0.5 | 1.1 | 1.4 | -0.6 | -0.1 | -0.1 | -0.4 | -0.1 | 1.1 | 0.4 | 0.1 | -0.8 | 0.6 | 0.3 | 0.5 | -1.2 | -0.9 | 0 | 0 | 0 | 0.3 | 1.3 | 1 | 0.4 | 2.3 | 2.2 | 2 | -0.3 | 0.3 | 1.3 | 0.8 | -0.5 | 0.5 | 0.5 | 1.7 | -0.3 | 0.4 | -0.5 | 0.2 | 0 | -0.2 | 0.2 | 0.7 | 0.4 | 0 | 0.4 | 1.9 | 1.8 | 3.4 | 0.1 | -0.3 | -0.2 | -1.4 | 1.1 | 1.4 | 1.9 | 0.8 | 0.6 | 1 | -0.4 | 2.6 | 4.2 | 1.1 | 1.6 | 0.3 | 0.5 | 0.4 | -2.7 | -0.1 | 0 | -1 | -0.4 | -0.8 | -1.6 | -1.5 | -0.2 | -0.6 | -0.3 | -1.3 | 0.6 | 0.5 | -0.5 | 3.5 | 2.7 | -0.1 | -0.6 | -0.7 | -0.8 | -2.3 | 0.2 | -0.4 | -0.8 | -0.1 | -0.2 | 0.3 | 0.5 | -1.7 | -0.3 | 0.9 | 0 | 0 | -0.3 | -0.4 | -0.6 | -2.7 | -2.1 | -3 | -3.1 | -0.9 | -0.4 | 0.5 | 0.5 | -0.1 | 0.6 | 0.5 | -0.6 | -0.1 | -0.1 | -0.3 | 0 | 0.2 | -0.2 | -0.6 | -0.2 | -0.3 | -1.4 | -0.1 | -0.2 | -4.9 | -10.8 | 4.2 | 2 | 0.7 | 0 | 0.3 | 0.3 | 0.1 | -0.1 | -2.1 | -0.1 | At3g25760 | 257641_s_at | AOC1 | encodes allene oxide cyclase. One of four genes in Arabidopsis that encode this enzyme, which catalyzes an essential step in jasmonic acid biosynthesis. Gene expression is induced during scenescence, a process that involves jasmonic acid signalling pathw | 6 | response to dessication | jasmonic acid biosynthesis | jasmonic acid biosynthesis | lipoxygenase pathway | Lipid signaling | 3.65 | 15.01 | ||||||||||||||||||||||||||
| At2g06050 | 0.709 | OPR3 | Encodes a 12-oxophytodienoate reductase that is required for jasmonate biosynthesis. Mutants are male sterile and defective in pollen dehisence. | -1.5 | 0 | 0 | 0.3 | -0.1 | 0.5 | -0.3 | -0.3 | 1.1 | 0.3 | -0.5 | 0.1 | 1.3 | -0.8 | 0.3 | 0.8 | -0.7 | -0.3 | 1 | -0.2 | -0.6 | 0.2 | -0.4 | 0.2 | 0 | -0.1 | -0.3 | 0 | 0.4 | 0.1 | 0.4 | 0.1 | 0.3 | -0.4 | -0.6 | -0.8 | -0.8 | -0.6 | -0.4 | -0.6 | -0.8 | -1.4 | -0.2 | 1.4 | 1.4 | 0 | 0.5 | 1.6 | -0.5 | 0.3 | 1.1 | -0.3 | 0 | -0.3 | -0.1 | -0.2 | 0 | -0.2 | 0 | -0.2 | -0.1 | -0.2 | 0 | 1.4 | 3.3 | 4.1 | 1 | 0.8 | -0.1 | -0.1 | -0.1 | 0.4 | 0.9 | -0.5 | 0.3 | 0.1 | 1 | 2.9 | -0.1 | 0.4 | 0 | 0 | 0 | 0.6 | 0.1 | 0.1 | -0.3 | 0 | -0.1 | -0.1 | -0.5 | -0.2 | -0.3 | -0.1 | 0 | -0.1 | 0.9 | 0.7 | -0.6 | 0 | -0.5 | -0.6 | -0.5 | 0.7 | 1.5 | 0.3 | -1.2 | -0.9 | -0.1 | 0.3 | -0.7 | 0.3 | -0.1 | 0 | -0.2 | -0.4 | -0.4 | 0.3 | 0 | 0.3 | 0 | 1.4 | 2.3 | 3.1 | 0.4 | 0.2 | 0 | -1.6 | 2.8 | 2.9 | 2.1 | 0.9 | 0.3 | 0.2 | -0.5 | 2.2 | 2.2 | 0.1 | 0.5 | 0 | -0.1 | 2.7 | -0.4 | 0.2 | -0.8 | -0.7 | -1 | -0.2 | 0.1 | -0.8 | -0.1 | -1.1 | -0.7 | -0.6 | -0.1 | -0.8 | -1.1 | 2.9 | 1.1 | -0.2 | -1.2 | -0.5 | -1.5 | -1.7 | 0.1 | -0.3 | -0.3 | -0.1 | -1 | -0.7 | -0.6 | -1.2 | -0.1 | 0 | -0.1 | 0 | -0.2 | -0.3 | -0.4 | -0.6 | -0.4 | -0.9 | -1.2 | -1 | -0.9 | -0.5 | -0.4 | -0.6 | -0.3 | -0.4 | -0.7 | -0.6 | -0.2 | 0.2 | 1.3 | 1 | -0.9 | -1 | 1 | 0 | -1.3 | 0.3 | -0.3 | -0.5 | -4.7 | -0.4 | -2.7 | 3.3 | -0.8 | -0.5 | -0.3 | -0.1 | -0.6 | -2.7 | -0.2 | At2g06050 | 265530_at | OPR3 | Encodes a 12-oxophytodienoate reductase that is required for jasmonate biosynthesis. Mutants are male sterile and defective in pollen dehisence. | 10 | response to wounding | 12-oxophytodienoate reductase activity | jasmonic acid biosynthesis | jasmonic acid biosynthesis | Lipid signaling | 3.47 | 8.85 | ||||||||||||||||||||||||||
| At3g45140 | 0.667 | LOX2 | Chloroplast lipoxygenase required for wound-induced jasmonic acid accumulation in Arabidopsis. | -3.1 | 0.2 | -0.1 | 0 | 0 | 0.2 | -0.1 | 0 | 0.1 | 0.2 | 0 | 0 | 0.3 | -0.1 | 0.2 | 0.1 | 0 | 0.1 | 0.2 | 0.1 | 0 | -0.3 | 0 | 0.2 | 0 | 0 | 0 | 0 | 0.2 | 0.1 | 0.2 | 0.1 | 0.4 | -0.2 | -0.4 | -0.1 | -0.1 | -0.1 | 0 | 0 | -0.4 | -0.3 | -0.4 | 1 | 0.7 | -0.1 | 0.2 | 0.9 | -0.2 | -0.1 | -0.3 | 0 | 0 | 0 | -0.3 | 0 | -0.2 | 0 | -0.2 | 0 | -0.1 | 0.1 | 0 | -0.4 | 0.3 | 1.8 | 2.1 | 1 | 0.3 | 0.7 | -0.1 | 0 | -0.1 | -0.1 | 0.3 | -0.2 | 0.5 | 0.6 | 0 | -0.3 | 0.4 | 0 | 0 | 0.9 | 0 | 0 | -0.1 | -0.2 | -0.3 | 0.1 | -0.2 | -0.6 | 0.2 | 0.4 | 0.3 | 0.1 | -0.1 | -0.3 | -0.1 | 0.1 | -0.2 | 0.1 | -0.1 | 0.2 | 1.4 | 1.1 | -1.3 | -2.1 | 0 | 0.2 | 0 | 0 | 0 | 0.2 | 0.2 | -0.1 | 0.8 | 1.4 | 0.4 | 1.4 | 0 | 0 | -0.1 | 0 | 0 | 0.4 | 0.3 | -0.8 | 1.1 | 0.9 | 2.9 | 1.8 | 0.6 | 1.8 | 0 | 0.1 | 0.8 | 0 | 0 | 0.4 | 0.1 | 0 | -0.8 | 0.5 | 0 | 0.2 | 0 | -0.3 | -1.5 | -2.2 | -1.2 | -0.1 | 0 | -0.1 | -0.2 | 0.1 | 0.2 | 1.7 | 1.7 | 0 | -0.3 | -0.1 | -0.5 | -1.5 | -0.4 | -0.3 | -0.7 | -0.3 | 0 | 0 | 0 | -0.2 | 0 | 0.1 | -0.6 | 0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.7 | -0.1 | 0 | 0.7 | 0 | -0.3 | -1 | -0.3 | -0.5 | -0.5 | 0.1 | 0.1 | -3 | 0.2 | 1.8 | -5 | -9.1 | 1.4 | -0.2 | 2.5 | 0.3 | -0.4 | 1.3 | -0.2 | 0 | -1.9 | 0 | At3g45140 | 252618_at | LOX2 | Chloroplast lipoxygenase required for wound-induced jasmonic acid accumulation in Arabidopsis. | 7 | response to wounding | response to jasmonic acid stimulus | lipoxygenase activity | jasmonic acid biosynthesis | abscisic acid biosynthesis | response to water deprivation | response to pest, pathogen or parasite | lipid, fatty acid and isoprenoid metabolism | stress response | jasmonic acid biosynthesis | lipoxygenase pathway | Lipid signaling | 2.54 | 12.09 | |||||||||||||||||||||||||
| At4g31780 | 0.666 | MGD1, MGDA | 1,2-diacylglycerol 3-beta-galactosyltransferase, putative / monogalactosyldiacylglycerol synthase, putative / MGDG synthase, putative, similar to MGD synthase type A from Arabidopsis thalian | -0.7 | 0 | -0.1 | 0.4 | -0.4 | 0 | -0.8 | -0.8 | 1.6 | -0.2 | -0.3 | 0.9 | 1.8 | -0.5 | 0.6 | 0.2 | -0.6 | -0.6 | -0.5 | 0 | -0.8 | -0.5 | -0.1 | 0 | -0.5 | -0.4 | -0.3 | 0.4 | 0 | -0.3 | -0.5 | -0.5 | -0.2 | -0.3 | -0.4 | 0 | 0 | 0 | -0.3 | 0 | -0.1 | -0.4 | -0.7 | -0.3 | -0.5 | 0 | -0.5 | -0.8 | -0.4 | -0.5 | -0.3 | -0.2 | 0 | 0 | -0.3 | 0 | -0.6 | 0 | -0.6 | -0.1 | -0.4 | -0.1 | 0 | 0.3 | 0.3 | 1.3 | 0.3 | 0.2 | -0.2 | -0.1 | 0.3 | 0.1 | 0.4 | -0.3 | 0 | 0.2 | 0.7 | 0.1 | 0 | 0 | 0.2 | 0.2 | -0.1 | -0.1 | 0 | 0.3 | -0.1 | 0.4 | 0 | 0.4 | 0.2 | 0.1 | 0.3 | 0.2 | -0.4 | -0.7 | 0.6 | 0.4 | 0 | 0.3 | 0 | 0.1 | -0.3 | -0.1 | 0 | 0.1 | -0.9 | -1.2 | -0.5 | 0.6 | 0.2 | 0.4 | 0.1 | 0.6 | -0.1 | -0.1 | 0 | -0.3 | -0.6 | -0.6 | 0 | 1.6 | 3 | 4.2 | 2.5 | 2.4 | 0 | 0 | 0.3 | 0.6 | 0.7 | 0.2 | -0.3 | -0.6 | 0 | 1.8 | 2.3 | 0.2 | 0 | 0.1 | -0.1 | 0.5 | -0.5 | 0 | 0.2 | 0 | 0 | 0 | 0.1 | -0.4 | -0.4 | -0.5 | -0.5 | -0.5 | -0.5 | -0.1 | -0.1 | 0.3 | -0.3 | 0 | 0.2 | -0.1 | 0 | -0.2 | 0.4 | 0.2 | 0 | -0.2 | 0 | -0.2 | -0.1 | 0 | 0.2 | 0.2 | -0.1 | 0.1 | 0 | -0.1 | -0.2 | 0 | 0 | 0 | -0.1 | -0.1 | -0.2 | -0.2 | 0 | -0.2 | 0.1 | 0.2 | -0.2 | 0.1 | 0 | 0.2 | 0 | -0.1 | -0.3 | -0.8 | 0 | 0 | 0 | -0.1 | -0.9 | -0.5 | -3 | 1.1 | -0.4 | 0.9 | -0.1 | 0 | 0 | -0.3 | -0.1 | -1.4 | -1 | At4g31780 | 253489_at | MGD1, MGDA | 1,2-diacylglycerol 3-beta-galactosyltransferase, putative / monogalactosyldiacylglycerol synthase, putative / MGDG synthase, putative, similar to MGD synthase type A from Arabidopsis thalian | 10 | UDP-glycosyltransferase activity | glycolipid biosynthesis | 1,2-diacylglycerol 3-beta-galactosyltransferase activity | galactolipid biosynthesis | chloroplast envelope | UDP-galactosyltransferase activity | lipid, fatty acid and isoprenoid metabolism | glycosylglyceride biosynthesis | Leaf Glycerolipid Biosynthesis | Leaf Glycerolipid Biosynthesis in Plastid | Synthesis of membrane lipids in plastids | 1.81 | 7.22 | ||||||||||||||||||||||||
| At1g19670 | 0.613 | ATCLH1 | Chlorophyllase is the first enzyme involved in chlorophyll degradation. It catalyzes the hydrolysis of the ester bond to yield chlorophyllide and phytol. AtCLH1 lacks a typical signal sequence for the chloroplast. | -4 | 0.5 | 0 | 0 | -0.1 | 0.3 | -0.7 | -0.8 | 0.8 | 0.2 | 0 | 0.7 | 0.8 | -0.2 | 0.5 | 0.2 | -0.2 | 0.3 | 0.4 | 0 | -0.2 | -1.3 | 0.2 | 0 | 0 | 0 | 0.1 | 0.4 | 0.3 | 0.3 | 0.1 | 0.5 | 0.2 | -0.5 | -0.9 | 0 | -0.1 | -0.4 | 0 | 0.2 | 0 | -0.8 | -0.2 | 1.9 | 1.9 | 0.4 | 0 | 1.6 | 0.3 | 1 | -0.8 | 0 | 0.2 | 0 | 0 | 0 | -0.1 | 0.2 | 0 | -0.1 | -0.3 | 0.2 | 0 | -0.1 | 1.3 | 2.6 | 0.9 | 1 | 0.6 | 0.5 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2.7 | -0.1 | 0.4 | 0.3 | 0 | 0.3 | 0.8 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | 0 | 0.4 | 0.1 | 0.1 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.2 | 0.2 | 1.2 | -0.8 | -2.7 | -2.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | -0.5 | 0.3 | -0.5 | -0.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0.5 | -0.3 | 1.8 | 1.3 | 2.3 | 1.2 | 1.3 | 1.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.9 | -1.9 | -0.4 | -2.7 | 0.5 | -0.1 | -0.7 | -2 | -3.6 | -4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.4 | 0 | 0 | 0.8 | -0.6 | -0.9 | -0.8 | -0.9 | -0.6 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.6 | 0 | -0.3 | 0.1 | -0.3 | -0.6 | -0.1 | 0 | 0.5 | -1.4 | 0 | -0.5 | 0 | -7.8 | 3.1 | 0.4 | 1 | 0.5 | 0.9 | 0 | 1.1 | 0 | -5.2 | 0 | At1g19670 | 255786_at | ATCLH1 | Chlorophyllase is the first enzyme involved in chlorophyll degradation. It catalyzes the hydrolysis of the ester bond to yield chlorophyllide and phytol. AtCLH1 lacks a typical signal sequence for the chloroplast. | 10 | chlorophyll catabolism | chlorophyllase activity | response to stress | Plastidial Isoprenoids (Chlorophylls, Carotenoids, Tocopherols, Plastoquinone, Phylloquinone) | Chlorophyll biosynthesis and breakdown | chlorophyll and phytochromobilin metabolism | chlorophyll catabolism | 2.71 | 10.96 | ||||||||||||||||||||||||||
| At4g08870 | 0.602 | similar to arginase (Arabidopsis thaliana) | -1 | 0.3 | -0.1 | 0 | -0.3 | -0.4 | -0.7 | -0.7 | 0.1 | -0.3 | 0 | 0.1 | 1 | -0.2 | 0.2 | 0.5 | -0.6 | -0.7 | 0.6 | 0 | -0.5 | -0.5 | 0.3 | 0 | 0.1 | 0 | -0.4 | 0 | 0.3 | 0.2 | 0.5 | 0.2 | -0.7 | -0.4 | -0.4 | -0.7 | -0.6 | -0.6 | -0.3 | -0.2 | -0.9 | -0.5 | -0.2 | 0.5 | 1.2 | -0.5 | -1.1 | 0 | -1.1 | 0 | -0.4 | -0.2 | 0.1 | -0.2 | -0.2 | -0.2 | -0.2 | -0.4 | -0.1 | -0.4 | -0.1 | 0 | -0.1 | 0 | -0.1 | 1 | 1.9 | 0.8 | 0.6 | -0.1 | 0.3 | 0 | 0.2 | 0.2 | 0 | 0.1 | 0.2 | 1.4 | 0.1 | 0 | 0.2 | 0.4 | 0 | 0.6 | 0.1 | 0.1 | 0 | 0 | -0.1 | 0 | -0.3 | 0 | 0.2 | 0.3 | 0.4 | 0.3 | -0.1 | 0.2 | 0.3 | 0.1 | 0.2 | 0.3 | 0 | 0.1 | 0.3 | 0.4 | -0.4 | -0.8 | -0.3 | -0.2 | -0.3 | 0 | 0 | 0.1 | 0 | -0.2 | 0 | 1 | 0.4 | 0.5 | -0.5 | 0 | -0.6 | -0.5 | 0 | -0.1 | 0 | 0 | 0.5 | 0.7 | 3.1 | 2.5 | 1.4 | 1 | 0.2 | -0.3 | 0 | 0.1 | 0.2 | 0.2 | 0.1 | 0.5 | -0.8 | 0.8 | -0.7 | 0.3 | -0.2 | 0.2 | 1 | 0.1 | -2.6 | -0.1 | 0.1 | 0.1 | -0.3 | -0.3 | -0.8 | 0.2 | 0.7 | 0 | 0.4 | 0.1 | -0.2 | -1.3 | -1 | 0 | 0 | 0.5 | 0.2 | -0.1 | 0 | -0.2 | 0.2 | 0.3 | 0.2 | 0 | -0.1 | -0.1 | -0.4 | -0.2 | -0.2 | 0.3 | -0.2 | 0.2 | 0 | 0 | 0.2 | 0.2 | 0.1 | 0 | 0 | 0.4 | 0.4 | -0.2 | -0.3 | 0.1 | 0 | -0.3 | -0.4 | 0 | -1 | 0.2 | 1.8 | -0.5 | -5.9 | 2.2 | -0.6 | 1.3 | 0.3 | 0.3 | 0 | -0.4 | 0.2 | -2.6 | 0 | At4g08870 | 255065_s_at | similar to arginase (Arabidopsis thaliana) | 2 | amino acid metabolism | spermine biosynthesis I | polyamine biosynthesis II | polyamine biosynthesis I | arginine degradation IX | arginine degradation VIII | arginine degradation XII | Arginine and proline metabolism | Urea cycle and metabolism of amino groups | Biosynthesis of Amino Acids and Derivatives | aspartate/ornithin cycle / nitric oxid from glutamate | 1.90 | 9.07 | |||||||||||||||||||||||||||
| At4g14680 | 0.601 | APS3 | ATP sulfurylase / sulfate adenylyltransferase 3 / ATP-sulfurylase 3 | -1 | 0 | -0.1 | 1.3 | 0 | 0.1 | -0.6 | -0.6 | -0.7 | -0.7 | -0.8 | -0.3 | -1.7 | -0.9 | -1.1 | -1.7 | -0.7 | 0.6 | -0.6 | -0.5 | -0.1 | -0.8 | -0.3 | -0.5 | -0.2 | -0.2 | -0.2 | 0 | -0.3 | 0.1 | 0 | -0.3 | 0 | -0.4 | -0.9 | -0.4 | -0.5 | -0.5 | -0.4 | -0.6 | -0.7 | -0.7 | -0.5 | 0.8 | 0.8 | -0.6 | 0.1 | 2.2 | 0.8 | 0.1 | 0.8 | 0.2 | -0.4 | 0 | -0.7 | 0.2 | -1.2 | 0 | -1.5 | 0.1 | -1 | 0.2 | -0.5 | -0.2 | 0.7 | 1.2 | 0.5 | 0 | 0 | 0.3 | 0 | 0.6 | 0.9 | -0.3 | 0.1 | 0.1 | 1.1 | 0.3 | -0.2 | 0.1 | 0.6 | -0.1 | 1.1 | 0.7 | 0.6 | 0.2 | -0.4 | 0.1 | 0 | 0 | -0.4 | 0 | 0.4 | -0.3 | -0.2 | -0.1 | 1.2 | 0.3 | -0.2 | 0.5 | 0.7 | 0.1 | -0.4 | 0.1 | 0.5 | -0.8 | -1 | -1.2 | 0.5 | 0.3 | -0.3 | 0 | -0.4 | 0 | 0 | -0.7 | 0 | -0.1 | 0.1 | -0.1 | 0.6 | 2 | 3.3 | 4.7 | 2.2 | 1 | 0.4 | -0.6 | 0 | 0.5 | 1.3 | 0.3 | 0.4 | 0.3 | -0.6 | 2 | 1.5 | 0 | 0.7 | 0.4 | 0.4 | -0.5 | -1 | 0.8 | -0.3 | -0.3 | 0.1 | 0.6 | -0.3 | -1.2 | -1.5 | -0.3 | -0.5 | 0 | 0.5 | 0.7 | 0.5 | -0.6 | 1 | 1 | -0.3 | -0.8 | -1.2 | -0.7 | 1 | -0.9 | -0.3 | 0 | -0.4 | -0.3 | -0.4 | -0.3 | -0.8 | 0 | -0.7 | 0 | 0.1 | 0 | -0.4 | 0.8 | 0 | 0.1 | -0.5 | 0 | -0.2 | 1.3 | 0.4 | 0 | 0 | -0.1 | 0.2 | -0.5 | -0.4 | 0.5 | 1.5 | -1.2 | 0 | -0.8 | 0 | -0.1 | -1 | -0.2 | -1 | 0 | -1 | 1.3 | 0.1 | 1.8 | 0.3 | 0.3 | -0.3 | -1.3 | 0.4 | -2.2 | 0.2 | At4g14680 | 245254_at | APS3 | ATP sulfurylase / sulfate adenylyltransferase 3 / ATP-sulfurylase 3 | 10 | sulfate adenylyltransferase (ATP) activity | sulfate assimilation | nitrogen and sulfur utilization | biogenesis of chloroplast | dissimilatory sulfate reduction | sulfate assimilation III | Sulfur metabolism | Purine metabolism | Selenoamino acid metabolism | Biosynthesis of Amino Acids and Derivatives | Glutathione metabolism | 2.49 | 6.90 | ||||||||||||||||||||||||
| At4g15440 | 0.595 | HPL1, CYP74B2 | Encodes a hydroperoxide lyase. Also a member of the CYP74B cytochrome p450 family. | -4.3 | -0.1 | 0 | 0 | -0.1 | 0 | -1.1 | -0.9 | -0.5 | -0.8 | -0.1 | 0 | 0.9 | 0 | -0.2 | 0.7 | -0.7 | -0.8 | 0.4 | -0.3 | -1 | -1.2 | 0 | -0.2 | -0.2 | 0.3 | -0.2 | 0.1 | -0.1 | 0.4 | 0.1 | 0.1 | 0.1 | -0.8 | -0.7 | -0.3 | -0.3 | -0.7 | 0.2 | 0 | -0.7 | -1.6 | -1 | 0.9 | 0 | -0.4 | 0 | -0.2 | -0.9 | 0.1 | -0.3 | -0.2 | 0.2 | -0.2 | 0 | -0.5 | -0.5 | 0 | -0.5 | -0.6 | -0.5 | 0 | 0 | -0.4 | 1.3 | 2.5 | 0.9 | 1.6 | 0.3 | 0.1 | 0.6 | 0.3 | -0.3 | 0 | 0 | -0.7 | 0.4 | 1.9 | 0 | 0.3 | 0.3 | 0.2 | 0.2 | 0.1 | 0.1 | -0.7 | -0.2 | 0 | -0.4 | 0.2 | 0.1 | 0.1 | 0.5 | 0.5 | 0.6 | 0.2 | 0 | -0.7 | -1 | 0.3 | 0 | -0.3 | -0.2 | 0.6 | 1.8 | 1.4 | -0.5 | -0.6 | 0.6 | -0.1 | -0.2 | 0.6 | 0.1 | 0.2 | 0.4 | 0.3 | 0.9 | 1.1 | 0.7 | 0.8 | 0.4 | 0.1 | 0.5 | 1.4 | 0.3 | 0.1 | 1.2 | -0.2 | 2.1 | 1.8 | 2.8 | 1.8 | 0.9 | 0.4 | 0.6 | 0.9 | 0.6 | 0 | 0.1 | -0.4 | -0.4 | -0.9 | -0.4 | 1.1 | 0.4 | 0.9 | 0.2 | 0.2 | 0 | -2.4 | -0.6 | 0.6 | -0.5 | -0.3 | 0.2 | 0.3 | 0.2 | -0.8 | -2.1 | 0 | -0.1 | 0.4 | -0.8 | -1.2 | -0.5 | -0.3 | -0.2 | -0.1 | 0.8 | 0.6 | -0.3 | 0 | 0.1 | 0.3 | 0.2 | 0.3 | 0 | 0 | 0 | 0.3 | 0.3 | 0.2 | 0.2 | 0 | 0.4 | 0 | -0.4 | -0.6 | 0 | 0.1 | 0.3 | 0.6 | 0.6 | -0.1 | 0 | -0.3 | -0.7 | -0.7 | 0.4 | 0 | -1.3 | -0.2 | -0.8 | 0 | -6.2 | 0.2 | -1.7 | 1.3 | 0.6 | 0.2 | 0 | 1.1 | 0 | -3.5 | 0 | At4g15440 | 245253_at | HPL1, CYP74B2 | Encodes a hydroperoxide lyase. Also a member of the CYP74B cytochrome p450 family. | 10 | lipid, fatty acid and isoprenoid metabolism | lipoxygenase pathway | Lipid signaling | oxylipin pathway | cytochrome P450 family, hydroperoxide lyase, oxylipin biosynthesis | 2.44 | 9.12 | ||||||||||||||||||||||||
| At1g20510 | 0.581 | 4-coumarate--CoA ligase family protein | -1.7 | -0.2 | -0.4 | 0.3 | -0.2 | 0.5 | -0.1 | -0.1 | 0.7 | 0.5 | -1.1 | 0.4 | -0.1 | -1.2 | -0.1 | 0.1 | -1.1 | 0.5 | 0.4 | -0.6 | 0.3 | 0 | -0.3 | 0 | 0.4 | 0.2 | 0 | -0.2 | 0 | 0.8 | 0.7 | 0.2 | 0 | -0.5 | -0.4 | -0.7 | -0.7 | -0.8 | -0.3 | -0.6 | -0.6 | -0.7 | -0.2 | 0.6 | 1 | -0.1 | -0.1 | 1 | 0.5 | 0.8 | 1.9 | -0.5 | 0 | -0.3 | 0 | -0.3 | 0.6 | -0.2 | 0.5 | -0.2 | 0.5 | -0.3 | 0 | 1.4 | 2.8 | 2.8 | 0 | 0.6 | 0 | 0.3 | -0.2 | 0 | 0 | -0.5 | -0.1 | 0 | 0.9 | 1.7 | -0.3 | -0.3 | -0.3 | 0 | 0 | 0.9 | 0 | -0.3 | -0.5 | -0.2 | -0.4 | -0.2 | -0.7 | -0.2 | -0.5 | -0.1 | 0.2 | 0.3 | 0.8 | 0 | -0.3 | 0 | -0.2 | 0 | -0.2 | 0.5 | 1 | 0.7 | 0 | 0.5 | 0 | -0.4 | -1.1 | -0.5 | -0.6 | -0.5 | -0.3 | -0.6 | -0.2 | 0.3 | 0.1 | 0.4 | 0 | 0.9 | 2.7 | 3.8 | 1.6 | 1 | 0.4 | -1.4 | 2.1 | 2.1 | 0.8 | 0.5 | 0.2 | 0.5 | -0.1 | 1.9 | 1 | -0.1 | 0 | -0.2 | 0 | 0.8 | -0.7 | 0.9 | -0.7 | -0.5 | -0.8 | 0 | 0.3 | 0.3 | 0.1 | -1 | -0.9 | -0.2 | 0.2 | 0 | -0.4 | 2 | 2.2 | 0.1 | -0.8 | -0.6 | -1.4 | -1.8 | -0.2 | -0.7 | -0.7 | 0.3 | -0.8 | -1 | -0.8 | -1.4 | -0.4 | -0.3 | -0.6 | -0.1 | -0.4 | -0.4 | -0.6 | -1.1 | -1 | -0.8 | -0.9 | -0.6 | -0.4 | -0.1 | -0.3 | -0.4 | -0.3 | -0.5 | -0.5 | -0.1 | 0.5 | 0.8 | 1.9 | 1.4 | 0.2 | 0.4 | 0.9 | 0.3 | -0.9 | 0.3 | -0.5 | -0.4 | -1.1 | -0.5 | -1.1 | 1.1 | -1 | 0 | -0.2 | -0.9 | -0.4 | -1.3 | -2 | At1g20510 | 259518_at | 4-coumarate--CoA ligase family protein | 2 | lignin biosynthesis | flavonoid biosynthesis | Phenylpropanoid pathway | Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase like | 2.92 | 5.93 | ||||||||||||||||||||||||||||
| At1g17420 | 0.578 | LOX3 | Lipoxygenase | -0.4 | -0.6 | -0.6 | -2.9 | -0.4 | -0.4 | -1 | -1 | 0.9 | 0.2 | -0.9 | 0.3 | 3.4 | -1.3 | 0.4 | 3 | -1.5 | -0.9 | 1.2 | -0.5 | 0.2 | 2 | -1 | 0 | -0.3 | -0.4 | -1.1 | -0.5 | 0.4 | -0.5 | -0.1 | -0.9 | 0.1 | -1.3 | -1.6 | -1.2 | -1.3 | -0.9 | -0.8 | -1 | -1 | -2.5 | -1 | 1 | 2.1 | -0.6 | -0.6 | 0.2 | 0 | 1 | 3.3 | -0.8 | -0.1 | -0.7 | -0.2 | -0.5 | 1.7 | -0.6 | 0.9 | -0.6 | 2.1 | -0.6 | 0.1 | 2.7 | 5.3 | 4 | 1 | -1.1 | -1.3 | -0.6 | -1.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 0.3 | 4.2 | 0.9 | -0.4 | 0.3 | -0.7 | -0.3 | 1.2 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 0.3 | -0.4 | 0.5 | -0.5 | -0.4 | 0.4 | 0.1 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 1 | 0.9 | 1.7 | 0 | -0.5 | 2.5 | 0.2 | 0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 1.3 | -0.6 | 0.5 | -0.2 | -0.3 | 1 | 0 | 2.5 | 4.3 | 5.1 | 3 | 3.1 | 1.2 | -1.1 | 5.6 | 3.5 | 2.1 | -0.3 | -0.4 | 0 | -0.7 | 3.6 | 3 | -0.6 | -0.6 | -0.6 | -0.6 | 4.4 | -1.8 | -0.6 | -1.7 | -0.6 | -1.7 | 3 | 2.1 | 0.8 | 0.3 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | 3.5 | 2.8 | -0.3 | -2.7 | 0.6 | -2.9 | 0.6 | 0 | -0.6 | -0.4 | -0.6 | -1.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.4 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.2 | 1.4 | 0 | 1 | -0.7 | -1.3 | -0.6 | 1.8 | -0.6 | -0.6 | 0.7 | -1.1 | -0.6 | -2.6 | 0 | -2.3 | 1.2 | -0.6 | -0.6 | -0.6 | -0.3 | -0.9 | -4.3 | -0.6 | At1g17420 | 261037_at | LOX3 | Lipoxygenase | 6 | defense response | jasmonic acid biosynthesis | response to wounding | growth | jasmonic acid biosynthesis | lipoxygenase pathway | Lipid signaling | 4.91 | 10.01 | ||||||||||||||||||||||||||
| At1g19570 | 0.578 | Similar to dehydroascorbate reductase from Oryza sativa | -0.5 | 0.1 | 0 | 0.1 | -0.3 | -0.1 | -0.6 | -0.6 | -0.1 | -0.6 | 0 | -0.1 | 0.6 | -0.2 | 0.2 | 0.3 | -0.3 | -0.4 | 0.3 | 0 | -0.5 | -0.9 | 0 | -0.1 | 0 | 0 | -0.4 | 0 | 0 | -0.2 | 0 | 0 | -0.3 | -0.4 | -0.7 | -0.6 | -0.3 | -0.2 | 0 | -0.1 | -0.8 | -1 | -0.9 | 0.5 | 0.7 | -0.1 | -0.3 | -0.1 | -1 | 0.1 | -0.4 | -0.3 | -0.2 | -0.2 | -0.6 | -0.3 | -0.5 | -0.1 | -0.4 | -0.3 | -0.3 | -0.1 | -0.2 | -0.1 | 0.8 | 1.9 | 1.5 | 0.8 | 0.4 | 0.7 | 0 | 0.2 | 0 | 0.5 | 0.2 | -0.2 | 0.2 | 0.2 | 0 | 0 | -0.2 | -0.2 | -0.4 | -0.1 | 0 | -0.2 | 0 | -0.4 | -0.2 | 0 | -0.1 | -0.2 | -0.3 | -0.1 | 0 | 0 | 0.4 | 0 | 0.1 | 0.2 | 0.2 | 0.5 | -0.3 | 0.2 | 0.7 | 1 | 1.1 | 1.2 | 0 | -0.3 | 0.1 | 0.4 | 0.6 | 0.6 | 0.2 | 0.2 | 0.9 | 1.2 | 1.3 | 1.3 | 0 | -0.2 | -0.2 | -0.7 | 0.5 | 0.3 | -0.1 | -0.6 | 0.9 | 1 | 1.6 | 1.4 | 0.9 | 0.6 | -0.3 | 0 | -0.5 | 0.2 | 0.6 | 0.4 | 0.2 | 0.1 | -0.4 | 0 | 0.7 | -0.1 | 0.1 | -0.7 | -0.8 | 0 | 0.3 | 0.4 | 0 | 0.4 | 0.6 | 0.4 | 0.5 | 1 | 0.7 | -0.3 | -0.1 | -0.2 | -0.2 | -0.8 | -0.3 | -1 | -0.1 | 0 | 0.1 | -0.2 | -0.5 | -0.6 | -0.8 | -0.5 | -0.3 | -0.1 | -0.2 | -0.3 | -0.2 | -0.3 | -0.3 | -0.1 | 0 | 0.1 | 0 | 0.5 | -0.2 | 0.1 | 0 | 0 | 0.2 | 0.4 | 0.1 | 0 | -0.9 | -0.6 | -0.2 | -0.6 | 1.1 | 0.5 | -0.6 | 0 | 0.7 | -0.4 | -3.6 | 1.5 | 0 | 0.3 | 0 | 0 | -0.2 | -0.3 | -0.4 | -3 | 1.1 | At1g19570 | 261149_s_at | Similar to dehydroascorbate reductase from Oryza sativa | 2 | ascorbate glutathione cycle | Glutathione S-transferase, Dehydroascorbate reductase family | 1.98 | 5.62 | |||||||||||||||||||||||||||||
| At3g01500 | 0.575 | CA1 | carbonic anhydrase 1, chloroplast / carbonate dehydratase 1 | -6.9 | 0.1 | 0.1 | 0.1 | 0.1 | 0 | 0 | 0 | -1.4 | -1 | 0 | 0 | -2.4 | -0.2 | -0.1 | -1.1 | 0.1 | 0.1 | -0.4 | 0 | -0.1 | -0.6 | 0 | 0 | -0.3 | -0.1 | 0 | 0 | 0 | -0.3 | -0.4 | -0.1 | 0.2 | 0 | -0.3 | 0.2 | 0.2 | 0.2 | 0.1 | 0.2 | 0.3 | 0.4 | -0.1 | 0 | -1.8 | 0.1 | -0.4 | 0 | -0.2 | -0.4 | 0.1 | 0.1 | 0 | 0.2 | -0.1 | 0.2 | -0.3 | 0.2 | -0.2 | 0.1 | -0.2 | 0.1 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | 0 | 0.2 | 0.1 | 2 | 1.4 | 0.1 | 0.1 | 0.1 | 1.3 | -0.1 | 0.1 | 0 | 0.3 | 0 | 0 | 0 | 0.1 | -0.4 | 0.1 | 0.1 | 1.3 | 0.1 | 0.2 | 0.1 | 0.2 | 0.1 | 0 | 0 | 0.1 | -0.4 | 0.7 | 1 | 1.7 | 0.1 | 0.1 | 0 | 0 | -0.3 | -1.2 | -2.9 | 0.1 | -0.4 | 0.1 | 0.1 | 0.1 | 0.1 | 0.3 | 0.3 | 0.2 | -0.2 | -0.4 | -0.5 | 0.1 | -0.4 | 2.9 | 4.8 | 3.3 | 3.3 | 0 | 0.2 | 0.2 | 0.1 | 0 | 0 | 0 | 0.2 | 0.1 | 0.1 | 3.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0 | -0.5 | -0.1 | -0.2 | 0.2 | 0.3 | 0.3 | 0.3 | 0 | 0 | 0.1 | -0.4 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.4 | 0.1 | 0.1 | 0.1 | 0.2 | 0.3 | 0.1 | -0.2 | 0 | 0.1 | 1.8 | 0.1 | -0.4 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | -0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0 | 0 | 0 | 0 | -0.4 | -0.2 | 0 | -0.1 | -0.1 | 0.1 | -0.1 | -0.2 | -8.5 | -10.3 | 2 | 0 | 1.3 | 0 | -0.2 | 0.1 | -0.2 | 0.1 | -0.1 | 0.1 | At3g01500 | 259161_at | CA1 | carbonic anhydrase 1, chloroplast / carbonate dehydratase 1 | 6 | cyanate degradation | Nitrogen metabolism | 1.96 | 15.11 | |||||||||||||||||||||||||||
| At1g52400 | 0.570 | BGL1 | encodes a member of glycosyl hydrolase family 1 | -2.2 | 0.5 | 0 | 0.7 | 0.1 | -0.1 | -0.6 | -0.8 | -0.4 | -1.1 | 0.4 | -0.1 | 0.1 | 0.3 | 0.1 | -0.4 | 0.3 | -0.3 | -0.4 | 0.4 | 0 | -1.8 | 0 | 0 | -0.1 | -0.4 | -0.1 | 0 | 0.3 | -0.1 | -0.1 | 0 | 0.1 | -0.7 | -1.3 | -0.3 | -0.4 | -0.6 | 0.3 | -0.4 | -1.5 | -1 | -1.2 | 1 | 0.2 | 0.1 | 0.3 | 0.4 | -0.1 | 0 | -0.8 | -0.1 | -0.1 | 0 | -0.4 | 0 | -0.5 | 0.1 | -0.4 | 0 | -0.5 | 0 | -0.4 | -0.1 | 0 | 1 | 0.9 | 1.1 | 0.5 | 1.1 | 0 | 1.3 | 2.6 | 3 | 2.3 | -0.4 | 1.6 | 0.8 | 0 | 0.2 | -0.8 | 0.2 | -0.3 | 0 | 0.1 | 0.2 | -0.2 | -0.6 | -0.3 | 0.2 | 0.2 | 0.2 | -0.6 | 0 | -0.2 | 0 | 0.9 | 1.1 | 0.6 | 1.5 | 1.2 | 0.8 | -1.2 | 0.5 | -0.3 | 0.4 | -0.4 | -1.5 | 0 | -0.2 | 0.1 | 0.9 | 0 | 2.7 | 0 | -0.1 | -0.7 | 0.2 | 0 | 0 | 0 | 0.1 | -0.2 | 0.4 | 0.6 | 1.9 | -0.8 | -0.3 | -0.1 | 0.2 | 1 | 1.3 | 0.8 | 1.2 | -0.5 | 0 | 0.2 | 1 | 1.2 | 1 | 0 | 0 | -1.2 | 0 | -0.6 | -0.3 | 0.2 | -0.9 | -0.6 | -0.3 | -0.2 | 0.7 | 0.8 | 1.7 | 1.6 | 0.1 | 0.6 | 1.7 | -0.5 | -0.9 | -0.4 | -0.6 | -0.4 | -1.7 | -1 | -1.9 | -0.9 | -0.6 | 0.2 | 0 | 0 | 0.2 | -0.5 | 0 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0.7 | 0.1 | 1.8 | 0.3 | 1.2 | 0.6 | 0.8 | -0.6 | 1 | -0.3 | 0.2 | -0.5 | -0.5 | -0.1 | -0.2 | -1.4 | 0.2 | -2.7 | -2.1 | -7 | 2.3 | -0.9 | 1.7 | 0 | 0 | 0 | 0 | -0.5 | -3.3 | 0.5 | At1g52400 | 259640_at | BGL1 | encodes a member of glycosyl hydrolase family 1 | 1 | Aminosugars metabolism | Nucleotide sugars metabolism | Glycan Biosynthesis and Metabolism | Glycoside Hydrolase, Family 1 | 2.99 | 10.12 | |||||||||||||||||||||||||||
| At5g36220 | 0.566 | CYP81D1 | cytochrome P450 family protein | 0.1 | -0.1 | -0.3 | -0.2 | -0.1 | 0.2 | -0.3 | -0.3 | 0.5 | 0.6 | 0.3 | -0.8 | 1.4 | 0.1 | 0 | 1.3 | -0.2 | 0 | 1.4 | 0.4 | -0.4 | 0.7 | 0.3 | 0.1 | 0 | -0.1 | -0.3 | -0.2 | 0.1 | 0.5 | 0.7 | 0.3 | -0.1 | -0.4 | -0.4 | -0.6 | -0.7 | -0.8 | 0 | -0.2 | -0.9 | -0.9 | -0.7 | 1.1 | 1.4 | -0.2 | -0.1 | 1.2 | -0.3 | 0.6 | -0.3 | -0.5 | -0.3 | -0.3 | 0 | 0.1 | 0.5 | 0 | 0.5 | 0 | 0.2 | -0.3 | -0.2 | -0.7 | 0.2 | 1.9 | 1.4 | 1.3 | 1.1 | 1.9 | -0.4 | -0.2 | 0 | -0.3 | 0 | 0.4 | 0.4 | 2.5 | -0.4 | -0.9 | -0.9 | -0.3 | -0.2 | 1.3 | -0.1 | -0.4 | -0.3 | -0.5 | -0.3 | -0.4 | -1 | -0.4 | -0.7 | 0.2 | 0.5 | 0.8 | 0.2 | 0 | -0.3 | -0.3 | -0.3 | -0.5 | 0 | 0 | 1.1 | 0.8 | 0.2 | 1.5 | -0.1 | -0.3 | -0.3 | -0.4 | 0.3 | 1 | -0.6 | -0.9 | -0.9 | 1.3 | 0.1 | 0.5 | -0.1 | -0.3 | 2.2 | 2.9 | 1 | 1.8 | 0 | -1.2 | -0.3 | -0.1 | 1.7 | 1.2 | 1 | 0.9 | -0.3 | -0.1 | -0.1 | 0 | 0 | -0.4 | -0.2 | 0 | -0.4 | -0.3 | -0.3 | -0.4 | -0.9 | -0.9 | -0.3 | -1.3 | 0 | -0.1 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.9 | -1 | -0.9 | -0.9 | -0.7 | -0.3 | -0.2 | -0.3 | -0.4 | -0.1 | -0.3 | -0.3 | 0.1 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.4 | -0.4 | -0.8 | -0.3 | -0.3 | -0.3 | -0.3 | 0 | 0.4 | -0.2 | 0.7 | 2 | -0.1 | 0.7 | -0.3 | -0.3 | -0.8 | 0.6 | 0.6 | 0.6 | -4.9 | 1.9 | 0.2 | 2.4 | -0.3 | -0.3 | 0.2 | -0.3 | -0.3 | -2.1 | -0.3 | At5g36220 | 246620_at | CYP81D1 | cytochrome P450 family protein | 1 | cytochrome P450 family | 2.41 | 7.88 | ||||||||||||||||||||||||||||
| At1g44350 | 0.563 | ILL6 | encodes a protein similar to IAA amino acid conjugate hydrolase. | -1 | -0.3 | -0.1 | -0.1 | -0.1 | 0.2 | -0.5 | -0.4 | 0.9 | 0.4 | -0.5 | 0.5 | 1.9 | -0.9 | 0.8 | 1.8 | -1 | -0.3 | 1.2 | -0.4 | -0.8 | 0.2 | -0.2 | -0.1 | -0.6 | -0.2 | -0.4 | 0 | 0.2 | 0 | 0 | 0 | -0.2 | -0.4 | -0.2 | -0.3 | 0 | -0.2 | -0.1 | 0 | -0.5 | -1.7 | -0.7 | 1 | 2.2 | -0.5 | -0.7 | 0.4 | -0.1 | -0.1 | -0.6 | -0.5 | 0 | -0.4 | -0.3 | -0.5 | 0.1 | -0.6 | 0 | -0.4 | 0.1 | -0.4 | 0.1 | -0.2 | 1.2 | 4 | 0.9 | 0.9 | 0.5 | 0.4 | -0.6 | 0.6 | 0.6 | -0.4 | -0.1 | 0.6 | 0.7 | 2.1 | -0.7 | -0.2 | -0.5 | -0.1 | 0 | 0.8 | -0.1 | -0.3 | 0 | 0 | -0.9 | -0.1 | -0.8 | -0.1 | -0.5 | -0.6 | -0.8 | -0.5 | 1 | 0.2 | -0.3 | 0 | -0.3 | -0.6 | -0.5 | 0.3 | 0.3 | 0 | 0.2 | 0.2 | -0.3 | 0.3 | 0 | 0.2 | 0.8 | 0.5 | -0.5 | -0.6 | -0.7 | 0.2 | 0.5 | 0.8 | 0 | 0.9 | 2.4 | 3.1 | 1.5 | 1.3 | -0.2 | -1.3 | 0.9 | 1.4 | 1.6 | 0.6 | 0.7 | 0.8 | -0.8 | 1.7 | 1.2 | 0 | 0 | -0.1 | -0.2 | 2.5 | 0.5 | -0.7 | -1.3 | -1.1 | -0.3 | -0.3 | -0.1 | 0.2 | -0.5 | -0.3 | -0.4 | -0.3 | -0.1 | -0.5 | -0.5 | 1.7 | -0.6 | 2.3 | -1.3 | -1 | -0.4 | 0 | -0.4 | -0.2 | -0.6 | -0.2 | -0.9 | -0.9 | -0.1 | -0.6 | -0.3 | -0.6 | -0.5 | -0.4 | 0 | 1.2 | 1.4 | 0.5 | 0.3 | 0.3 | 0.6 | 0.3 | -0.6 | -0.5 | -0.8 | -0.3 | -0.1 | -0.7 | -0.2 | -1.3 | -0.8 | -0.1 | 1.1 | 0.5 | -0.9 | -0.2 | -0.2 | 0.8 | 0.2 | -0.3 | -0.6 | -0.5 | -1.4 | -0.5 | -1.7 | 1.1 | -0.8 | 0.1 | -0.3 | 0.2 | -0.2 | -1.9 | -0.7 | At1g44350 | 245244_at | ILL6 | encodes a protein similar to IAA amino acid conjugate hydrolase. | 4 | auxin metabolism | IAA-Ala conjugate hydrolase activity | 2.74 | 5.93 | ||||||||||||||||||||||||||||
| AtCg00570 | 0.563 | PSBF | PSII cytochrome b559 | -1.1 | 0.1 | 0.1 | 0.9 | 0 | 0 | 0.1 | 0.1 | 0.1 | 0.1 | 0 | 0.1 | -0.5 | -0.2 | 0 | -0.6 | 0 | 0.2 | -0.1 | 0 | 0 | -0.5 | -0.3 | -0.3 | 0.2 | 0.1 | 0 | 0 | 0.3 | 0.3 | 0 | 0.1 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.2 | -0.2 | -0.1 | 0 | -0.3 | 0.1 | -0.1 | -0.2 | 0.1 | 0 | 0.1 | 0.2 | 0.1 | 0.2 | -0.1 | 0 | 0 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0.1 | 0.3 | -0.2 | -0.1 | 0 | 0.7 | 0.6 | 0.3 | 0 | 0.1 | 0 | 0.2 | 0 | 0.1 | 0.2 | 0.3 | -0.1 | 0.2 | 0.3 | 0.2 | 0.3 | 0.4 | 0.2 | 0.3 | 0 | 0.1 | 0.2 | 0.1 | -0.1 | 0.1 | 0.3 | 0.1 | 0 | 0 | -0.1 | 0.1 | 0 | 0 | -0.2 | 0 | 0 | 0.4 | 0.7 | 0.7 | 0.5 | 0 | 0.2 | 0 | -0.3 | -0.2 | 0 | 0.1 | 0.1 | -0.5 | -0.1 | 0.3 | 0.6 | 0 | 0 | 0.3 | 0.1 | 0 | 0 | 0 | 0.3 | 0 | 0.3 | 0.5 | 0.2 | 0.5 | 0.1 | -0.2 | -0.1 | 0 | -0.3 | -0.2 | -0.3 | 0 | 0 | 0 | 0 | -0.1 | 0.2 | 0 | -0.1 | 0.2 | -0.1 | 0.3 | 0.2 | 0.4 | 0 | -0.5 | -0.3 | 0.1 | 0.2 | -0.4 | -0.2 | -0.4 | -0.4 | -0.3 | 0.2 | -0.1 | 0.3 | 0 | 0.1 | -0.5 | -0.5 | 0.3 | 0 | -0.1 | -0.3 | -0.2 | 0 | 0 | 0.1 | -0.3 | 0.1 | -0.2 | 0.1 | 0 | 0.1 | 0 | -0.3 | -0.1 | -0.1 | -0.3 | -0.9 | -0.5 | 0 | -0.3 | 0 | 0.1 | -0.2 | -0.1 | -2 | -5.3 | 1.9 | 0.5 | 1 | -0.3 | -0.2 | 0.5 | -0.1 | 0.2 | 0 | 0.8 | AtCg00570 | 244963_at | PSBF | PSII cytochrome b559 | 6 | Photosystems | Photosystem II | Photosystem II reaction center | 1.07 | 7.22 | ||||||||||||||||||||||||||||
| At3g44300 | 0.562 | NIT2 | encodes a nitrilase (nitrile aminohydrolase, EC 3.5.5.1) which catalyzes the hydrolysis of indole-3-acetonitrile (IAN) to indole-3-acetic acid (IAA).Mutants have reduced sensitivity to IAN and are sensitive to IAA. Other members of the NIT gene family a | 0 | 0 | 0.1 | -0.5 | -0.3 | -0.3 | -0.2 | -0.1 | 0.1 | 0 | -0.2 | -0.1 | 0.2 | 0 | 0.1 | 0.2 | 0 | -0.1 | 0 | -0.1 | -0.1 | -0.2 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0.1 | 0 | -0.3 | -0.2 | -0.1 | -0.2 | 0 | -0.2 | -0.1 | -0.4 | -0.3 | -0.4 | 0.5 | 1 | -0.1 | -0.1 | 0.4 | -0.2 | -0.2 | -0.2 | 0 | 0 | 0 | -0.1 | 0 | -0.2 | 0 | -0.2 | -0.1 | -0.4 | 0.1 | -0.1 | 0.1 | -0.3 | 0.1 | 0.3 | -0.1 | 0.1 | 0.1 | -0.5 | 0.1 | 0.2 | 0 | 0.6 | -0.4 | 0.3 | 0.1 | 0 | 0 | 0 | -0.1 | -0.2 | 0.1 | 0.1 | 0.5 | -0.3 | 0.1 | 0.2 | 0.4 | -0.3 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | 0.4 | -0.6 | 0 | -0.1 | 0.1 | 0 | -0.1 | -0.1 | -0.2 | -0.4 | 0.2 | -0.2 | 0.2 | 0.4 | 1.2 | 1.1 | 1.3 | -0.1 | 0 | 0 | 0.2 | 0 | 0.4 | -0.1 | 0.2 | 0.5 | 0.8 | 0.9 | 1.2 | 0.1 | 0.2 | 0 | -0.2 | 0.3 | 0.2 | 0.1 | 0.1 | -0.4 | -0.1 | 0 | 0 | 0.8 | 0.1 | 0.1 | -0.1 | 0.8 | 0 | -0.6 | 0.1 | -0.1 | 0.1 | 0 | -0.5 | -1.1 | -0.1 | 0.2 | -0.3 | 0.2 | -0.2 | -0.2 | -0.5 | 0.1 | -0.2 | 0.2 | -0.1 | -0.2 | -0.2 | -0.1 | -0.2 | -0.3 | 0 | -0.2 | 0 | 0 | -0.8 | -0.2 | 0.1 | 0.3 | 0 | 0 | 0.1 | 0 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.4 | 0.2 | 0.5 | -0.3 | -0.1 | -0.2 | 0 | 0.2 | 0 | -0.4 | -0.5 | -0.4 | -0.3 | -0.2 | -0.7 | -0.1 | -0.5 | 0.1 | 0.7 | 0.1 | -6.7 | 6.4 | 4.3 | 0 | 0 | 0 | 0.7 | 0.2 | -0.3 | -1 | 0 | At3g44300 | 252678_s_at (m) | NIT2 | encodes a nitrilase (nitrile aminohydrolase, EC 3.5.5.1) which catalyzes the hydrolysis of indole-3-acetonitrile (IAN) to indole-3-acetic acid (IAA).Mutants have reduced sensitivity to IAN and are sensitive to IAA. Other members of the NIT gene family a | 9 | nitrilase activity | response to pathogenic bacteria | indoleacetic acid biosynthesis | plant / fungal specific systemic sensing and response | plant hormonal regulation | IAA biosynthesis I | Nitrogen metabolism | Tryptophan metabolism | Cyanoamino acid metabolism | Benzoate degradation via CoA ligation | 1.30 | 13.22 | |||||||||||||||||||||||||
| At3g44310 | 0.562 | NIT1 | nitrilase 1. Mutants are resistant to indole-3-acetonitrile. NIT1 catalyzes the terminal activation step in indole-acetic acid biosynthesis. Predominantly expressed isoform of nitrilase isoenzyme family | 0 | 0 | 0.1 | -0.5 | -0.3 | -0.3 | -0.2 | -0.1 | 0.1 | 0 | -0.2 | -0.1 | 0.2 | 0 | 0.1 | 0.2 | 0 | -0.1 | 0 | -0.1 | -0.1 | -0.2 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0.1 | 0 | -0.3 | -0.2 | -0.1 | -0.2 | 0 | -0.2 | -0.1 | -0.4 | -0.3 | -0.4 | 0.5 | 1 | -0.1 | -0.1 | 0.4 | -0.2 | -0.2 | -0.2 | 0 | 0 | 0 | -0.1 | 0 | -0.2 | 0 | -0.2 | -0.1 | -0.4 | 0.1 | -0.1 | 0.1 | -0.3 | 0.1 | 0.3 | -0.1 | 0.1 | 0.1 | -0.5 | 0.1 | 0.2 | 0 | 0.6 | -0.4 | 0.3 | 0.1 | 0 | 0 | 0 | -0.1 | -0.2 | 0.1 | 0.1 | 0.5 | -0.3 | 0.1 | 0.2 | 0.4 | -0.3 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | 0.4 | -0.6 | 0 | -0.1 | 0.1 | 0 | -0.1 | -0.1 | -0.2 | -0.4 | 0.2 | -0.2 | 0.2 | 0.4 | 1.2 | 1.1 | 1.3 | -0.1 | 0 | 0 | 0.2 | 0 | 0.4 | -0.1 | 0.2 | 0.5 | 0.8 | 0.9 | 1.2 | 0.1 | 0.2 | 0 | -0.2 | 0.3 | 0.2 | 0.1 | 0.1 | -0.4 | -0.1 | 0 | 0 | 0.8 | 0.1 | 0.1 | -0.1 | 0.8 | 0 | -0.6 | 0.1 | -0.1 | 0.1 | 0 | -0.5 | -1.1 | -0.1 | 0.2 | -0.3 | 0.2 | -0.2 | -0.2 | -0.5 | 0.1 | -0.2 | 0.2 | -0.1 | -0.2 | -0.2 | -0.1 | -0.2 | -0.3 | 0 | -0.2 | 0 | 0 | -0.8 | -0.2 | 0.1 | 0.3 | 0 | 0 | 0.1 | 0 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.4 | 0.2 | 0.5 | -0.3 | -0.1 | -0.2 | 0 | 0.2 | 0 | -0.4 | -0.5 | -0.4 | -0.3 | -0.2 | -0.7 | -0.1 | -0.5 | 0.1 | 0.7 | 0.1 | -6.7 | 6.4 | 4.3 | 0 | 0 | 0 | 0.7 | 0.2 | -0.3 | -1 | 0 | At3g44310 | 252678_s_at (m) | NIT1 | nitrilase 1. Mutants are resistant to indole-3-acetonitrile. NIT1 catalyzes the terminal activation step in indole-acetic acid biosynthesis. Predominantly expressed isoform of nitrilase isoenzyme family | 9 | nitrilase activity | indoleacetic acid biosynthesis | plant / fungal specific systemic sensing and response | plant hormonal regulation | IAA biosynthesis I | 1.30 | 13.22 | ||||||||||||||||||||||||||
| At3g44860 | 0.554 | S-adenosyl-L-methionine:carboxyl methyltransferase family protein, similar to defense-related protein cjs1 (Brassica carinata) | -3.9 | 0 | -1.4 | -0.6 | -0.3 | 0 | -0.5 | -0.5 | 0.7 | 0.2 | -0.4 | -0.3 | 0.3 | -0.9 | 0 | 0.4 | -0.8 | -0.2 | 0.5 | -0.3 | -0.8 | 0 | -0.5 | 0.2 | 0.2 | -0.1 | -0.5 | -0.5 | 0.4 | 0.7 | 0.5 | -0.4 | -0.5 | -0.8 | -1.6 | -1.2 | -1.2 | -0.9 | -0.3 | -0.8 | -0.8 | -1.7 | -0.9 | 0.8 | 1.2 | -0.4 | -1.4 | 0.9 | -1.2 | 1.8 | 0 | -1 | -0.3 | -0.7 | -0.3 | -0.5 | -0.4 | -0.5 | -0.3 | -0.5 | -0.2 | -0.7 | -0.3 | -0.4 | 2.1 | 3.5 | 0.9 | 2.4 | 3.3 | 0 | -2.3 | 2.1 | 0.9 | -1.1 | -0.1 | -1.3 | 2.2 | 6.7 | -1.6 | -1.4 | -0.6 | -0.4 | 1.5 | 0.9 | 1.2 | 0.5 | -1.5 | -0.8 | -0.8 | -0.1 | -1.6 | -1.4 | -1.4 | 0 | 0.7 | -0.4 | 3 | 2.3 | -1.5 | 0.1 | -1.1 | -0.6 | -1.1 | 0 | 3.3 | 2.1 | 3 | 1.3 | 1.9 | 1.9 | -1.3 | 0.1 | -0.7 | 0.6 | -0.6 | -1.4 | 1.3 | 2.6 | 3.5 | 0.7 | 1.8 | 4.4 | 6.4 | 7.8 | 6.3 | 6.6 | 0.5 | -4 | 2.1 | 1 | 1.9 | 1.4 | 3.2 | 0.7 | -2.1 | 4.8 | 4.8 | 1.4 | 0 | -1 | -0.3 | 0.3 | -2.5 | -0.6 | -0.2 | -1.7 | -2.1 | -1.2 | -1.2 | 1 | -2.7 | -0.5 | -0.9 | -1.9 | -0.3 | -1 | -0.6 | 2.8 | 0.7 | -0.6 | -3 | -1.2 | -4.4 | -3.1 | -1.5 | -1.7 | -0.5 | -0.7 | -1.9 | -0.4 | 0.6 | -1.2 | -0.8 | -0.5 | -0.9 | -0.2 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -0.6 | -1.8 | 2.1 | 1.8 | -1 | -1.1 | -1.2 | -0.6 | -1.1 | -0.1 | 0.6 | 2.7 | 2.2 | 1.5 | -0.2 | 1.2 | 0.5 | -3.6 | 0 | -1.5 | -0.6 | -1.9 | -2 | -4.5 | 0.8 | -0.8 | -0.6 | -0.5 | -0.1 | 0 | -2.9 | -0.6 | At3g44860 | 246340_s_at | S-adenosyl-L-methionine:carboxyl methyltransferase family protein, similar to defense-related protein cjs1 (Brassica carinata) | 2 | Methyltransferase, SABATH family | 5.53 | 12.34 | ||||||||||||||||||||||||||||||
| At4g18440 | 0.541 | similar to Adenylosuccinate lyase (Adenylosuccinase) (Escherichia coli) | -0.4 | -1.2 | 0 | -0.3 | 0 | -0.1 | -0.5 | -0.3 | -0.2 | -0.7 | -0.1 | 0.2 | 0.3 | -0.3 | -0.2 | 0.6 | -0.4 | -0.6 | 0.3 | 0 | -0.4 | -1.4 | 0.1 | -0.1 | 0.2 | -0.3 | -0.1 | 0 | 0.4 | 0.5 | 0 | 0.5 | -0.4 | -0.1 | -0.1 | -0.1 | -0.2 | 0 | 0.2 | 0.2 | -0.3 | -0.3 | -0.2 | 0.2 | 0.1 | 0.4 | 0.4 | 0 | -1.2 | 0.3 | 0 | 0 | 0.2 | 0 | -0.3 | 0.1 | -0.5 | 0.3 | -0.3 | 0.2 | -0.3 | 0.3 | 0 | -0.1 | 0.3 | 1 | 1.7 | 0.3 | 0.6 | -0.4 | 0 | 0.2 | 0 | 0 | -0.5 | 0 | 0.1 | 0.1 | 0.6 | 0.2 | 0.5 | 0.1 | 0.2 | 0.6 | 0.2 | 0.3 | -0.1 | -0.1 | 0 | -0.2 | 0 | 0.1 | 0.3 | 0 | 0 | 0 | 0.2 | 0 | 0 | -0.3 | -0.1 | -0.4 | 0 | 0.2 | 0.2 | -0.3 | -1.5 | -2.1 | 0.4 | 0 | -0.4 | -0.8 | -1 | -0.7 | 0.2 | 0 | -0.1 | 0.8 | 0.2 | -0.1 | 0.1 | 0 | -0.1 | -0.2 | -0.6 | -0.3 | -0.2 | -0.3 | 1 | 0.9 | 3.2 | 1.5 | 1.1 | 1.2 | 0 | 0.2 | 0.2 | 0.1 | -0.1 | 0.3 | 0.1 | -0.1 | -0.3 | 0.2 | 0.2 | 0.3 | 0 | -0.6 | -0.6 | 0.1 | -0.9 | 0.2 | 0.2 | -0.2 | 0 | -0.3 | -0.4 | 0 | 1.7 | 0 | 0.2 | 0.3 | -0.2 | -1.2 | 0.5 | 0.4 | -0.1 | 0.1 | 0.1 | 0.3 | 0 | -0.6 | -0.4 | -0.1 | 0.1 | 0 | -0.2 | -0.3 | -0.3 | -1.4 | -0.8 | 0.2 | 0.4 | 0.2 | 0.1 | 0.2 | 0 | 0.1 | -0.5 | 0 | -0.4 | 0.2 | 0.1 | 0.5 | -0.7 | -0.5 | 0 | -0.5 | 0 | 0.8 | -0.5 | 0 | -0.6 | 0.7 | -3.2 | 3.3 | -0.3 | 1 | 0.6 | 0.3 | 0.4 | 0.6 | -0.2 | -2.6 | 0.9 | At4g18440 | 256461_s_at | similar to Adenylosuccinate lyase (Adenylosuccinase) (Escherichia coli) | 2 | nucleotide metabolism | de novo biosynthesis of purine nucleotides I | de novo biosynthesis of purine nucleotides II | phenylalanine degradation I | mixed acid fermentation | acetyl-CoA assimilation | TCA cycle variation VII | TCA cycle variation VIII | TCA cycle variation II | TCA cycle variation IV | TCA cycle -- aerobic respiration | Nucleotide Metabolism | Purine metabolism | Alanine and aspartate metabolism | 1.80 | 6.60 | ||||||||||||||||||||||||||||
| At5g05600 | 0.536 | oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to flavonol synthase (Citrus unshiu) and to leucoanthocyanidin dioxygenase (Daucus carota) | -3.4 | 0.6 | 0.3 | -3 | -0.2 | 0.2 | -0.2 | -0.1 | 0.3 | 0.1 | -0.4 | -0.3 | 0.9 | -0.8 | 0 | 0.5 | -0.7 | 0 | -0.1 | -0.3 | -0.5 | -0.2 | 0 | 0 | -0.2 | 0.4 | -0.7 | 0.1 | 0.1 | -0.1 | 0.2 | 0 | -0.4 | -0.7 | -0.8 | 0 | -0.4 | -0.4 | -0.4 | -0.2 | -0.4 | -1.9 | -0.4 | 2 | 2.6 | -0.8 | -2.9 | 1.8 | 1.9 | 0.8 | -1 | -0.5 | 0 | -0.4 | -0.2 | -0.6 | 0 | -0.6 | -0.2 | -0.6 | 0.1 | -0.5 | 0 | 0 | 2.5 | 4.8 | 3.4 | 3.3 | 2.6 | 2.2 | -0.4 | 0.4 | 0.3 | 0 | 0.8 | 1.7 | 2 | 3.1 | -1.2 | -0.2 | -0.4 | -0.4 | 0 | 1.1 | 0.2 | -0.5 | 0 | 0.5 | 0.6 | 1.1 | -1.2 | -0.8 | -0.4 | -0.4 | -0.4 | -0.4 | 0.9 | 0 | 0 | 0.1 | 0.6 | 0.7 | -0.8 | 0.3 | 0.6 | 0.6 | 0.7 | 1.7 | -0.5 | -0.6 | -0.1 | 0.6 | 1.4 | 1.7 | -1.2 | -0.8 | -0.4 | -0.4 | 0.3 | 0.6 | -0.4 | 0.5 | 1.7 | 2 | 1.5 | 1.5 | -2.1 | -1.6 | 0.4 | 0.9 | 2.1 | 1.8 | 1.5 | 0.7 | -1.9 | 1.1 | 0.7 | 0.6 | 1.2 | 1.1 | 0.9 | 4.4 | 2.8 | -0.4 | -2.1 | -1.2 | -0.8 | -0.4 | -0.4 | 0 | -0.4 | -1.1 | -1.5 | -0.7 | -0.3 | 1 | 1.5 | 3.9 | -0.4 | -0.4 | -1.6 | -1.2 | -0.8 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -2.4 | -1.5 | -0.7 | -1.8 | -2 | -1.3 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | -1 | -0.4 | -1.4 | -0.5 | -0.3 | 0.2 | 0.8 | -0.8 | -1.2 | -0.8 | 0.8 | 0.1 | -0.4 | -0.4 | -0.4 | -0.4 | -0.4 | 0.6 | 0.3 | -0.4 | -4.3 | 0.2 | -3.6 | 2.9 | 0.9 | 1.3 | -0.2 | -0.2 | -0.5 | -3.5 | -0.4 | At5g05600 | 250793_at | oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to flavonol synthase (Citrus unshiu) and to leucoanthocyanidin dioxygenase (Daucus carota) | 2 | Phenylpropanoid Metabolism | Flavonoid and anthocyanin metabolism | Gibberellin metabolism | giberelin biosynthesis | 4.30 | 9.17 | |||||||||||||||||||||||||||||
| At4g03050 | 0.534 | AOP3 | encodes a 2-oxoglutarate-dependent dioxygenase that catalyzes the conversion of methylsulfinylalkyl glucosinolates to hydroxyalkyl glucosinolates. involved in glucosinolate biosynthesis and secondary metabolism. | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.8 | 0 | 0 | 0 | 0 | -0.4 | 0 | 0 | 0 | 0 | 0 | 0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.8 | 0 | 0 | -8.4 | 8.1 | 2.8 | 0 | 0 | 0 | -1.1 | 0 | 0 | 0 | 0 | At4g03050 | 255471_at | AOP3 | encodes a 2-oxoglutarate-dependent dioxygenase that catalyzes the conversion of methylsulfinylalkyl glucosinolates to hydroxyalkyl glucosinolates. involved in glucosinolate biosynthesis and secondary metabolism. | 10 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors | glucosinolate biosynthesis | secondary metabolism | glucosinolate biosynthesis from homomethionine | Glucosinolate Metabolism | 0.00 | 16.63 | |||||||||||||||||||||||||
| At3g22740 | 0.531 | HMT3 | homocysteine S-methyltransferase 3 | -3 | 0.7 | 0.5 | 0.2 | -0.9 | -0.9 | -0.9 | -0.9 | 0.2 | -0.2 | -0.8 | 0.4 | 1.8 | -1 | -1.2 | 1.2 | -1.4 | -1 | 0.7 | -0.2 | -1.1 | -0.2 | 0.3 | -0.5 | 1.1 | 0.2 | 0.3 | 0.2 | -0.4 | 0 | 0 | 0.6 | 0.3 | 0.2 | -0.7 | -0.6 | -0.4 | 0 | 0.1 | -0.4 | -1.2 | -1.2 | -1 | 1.5 | 0.5 | 0.5 | -1 | 0.2 | 0 | 0.9 | -0.2 | -0.6 | 0.2 | -0.9 | 0.2 | -0.3 | 0.2 | -0.2 | 0.2 | -0.6 | 0.2 | -0.4 | 0.2 | 0 | -0.1 | 1.6 | 0.2 | 0.9 | 1.1 | 1.3 | 0.2 | 0.9 | 0.9 | 0.8 | 0.7 | 0.8 | 1.5 | 0.3 | 0.1 | 0 | -0.1 | -0.1 | 1 | 0.8 | 0.7 | 0.5 | 0.4 | -0.1 | -0.3 | 0.2 | 0 | -0.3 | -0.6 | -0.8 | -0.5 | -0.1 | 0.9 | 0.9 | 0.5 | -0.5 | -0.6 | -0.2 | -0.7 | 0 | -0.5 | 0 | 1.6 | 1.7 | 0.1 | 0 | 0 | -0.6 | 0.2 | 1.2 | 0.2 | -0.9 | -0.8 | -0.6 | 0.5 | 0 | 0.3 | 0.2 | 0.9 | 0 | 0.4 | -0.1 | 0.3 | -1.4 | -0.4 | 0.4 | 0.8 | 1.9 | 1.4 | 0.9 | -0.4 | 0.8 | 0.3 | 1 | 0.1 | 0.1 | 0.8 | 0.1 | -0.5 | 1.1 | -1.3 | -0.6 | 0 | -1.4 | -0.4 | -0.1 | -1.1 | 0 | 0.1 | 0.8 | -0.3 | -0.4 | -0.1 | 0.2 | 2.1 | 0.2 | -0.6 | -1.4 | -0.9 | -2.1 | -1.8 | -1.7 | 0 | 0.2 | 0 | 0.5 | 0.6 | 0.1 | -0.3 | -0.4 | -0.4 | 0.4 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 0.3 | -0.2 | -0.6 | 0.1 | -0.1 | -0.1 | 0 | 0 | -0.5 | -0.2 | -1 | -1.6 | 0.2 | -0.7 | 0.2 | 0.2 | 0.2 | 0 | -0.5 | 0.3 | -3.4 | 3.4 | 0.7 | 0.4 | 0.2 | 0.2 | -1.7 | -0.4 | 0.2 | -1.9 | 0.2 | At3g22740 | 258322_at | HMT3 | homocysteine S-methyltransferase 3 | 6 | methionine biosynthesis II | Methionine metabolism | Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate | 2.69 | 6.89 | ||||||||||||||||||||||||||
| At2g14750 | 0.528 | APK | adenylylsulfate kinase 1 (AKN1) / adenylylsulfate kinase 1, chloroplast precursor (APS kinase, Adenosine-5'phosphosulfate kinase, ATP adenosine-5'- phosphosulfate 3'-phosphotransferase) | -2.2 | 0.4 | 0.1 | -0.2 | 0.3 | 1 | 0.6 | 0.4 | 0.4 | 0 | -0.2 | 0.4 | 0.4 | -0.5 | 0.7 | 0 | -0.5 | 0.6 | 0 | 0.1 | 0.7 | -0.3 | 0 | -0.2 | -0.1 | -0.1 | -0.3 | 0.4 | -0.1 | 0.1 | 0.3 | 0.1 | 0.4 | -0.3 | -0.7 | -0.5 | -0.4 | -0.1 | -0.2 | -0.3 | -0.5 | -0.3 | -0.1 | 1.1 | 0.6 | 0 | -0.5 | 1.3 | 0.1 | 0.6 | 0.2 | 0 | 0.1 | 0.1 | -0.2 | 0.4 | -0.4 | 0.3 | -0.5 | 0.3 | -0.5 | 0.1 | -0.1 | 0 | 0.1 | 0.8 | 0.1 | 0.6 | -0.1 | 0.2 | 0.1 | 0.3 | 0.4 | 0.1 | 0.3 | 0.4 | 0.8 | 0.2 | 0 | 0 | 0.1 | 0.4 | 0.4 | 0.3 | 0.3 | -0.1 | 0 | 0.1 | -0.3 | 0.5 | -0.1 | -0.4 | -0.1 | -0.1 | -0.2 | 0.3 | 0.7 | 0 | 0.2 | 0.5 | 0.3 | 0.6 | -0.3 | -0.4 | 0.1 | 0.2 | -0.3 | -0.2 | -0.3 | -0.6 | -0.2 | 0.1 | 0 | 0.9 | 0.3 | -0.1 | -0.2 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | 0.4 | 0 | 0.3 | 0.4 | 0.1 | 0.4 | 0.3 | 0.7 | 1.2 | 0.2 | 0.3 | -0.4 | 0.5 | -0.1 | 0.2 | 0.9 | 0.7 | 0.7 | -0.3 | -1 | 0.9 | 0 | 0.2 | 0.2 | -0.1 | 0.2 | -0.2 | -2.3 | -0.2 | -0.8 | 0 | 0 | -0.8 | -1.7 | 0 | 0.8 | 2.2 | 0.2 | -0.3 | -1.4 | -2.3 | -0.2 | -0.6 | 0 | 0.3 | 0 | -0.2 | -1.1 | -0.9 | -0.1 | 0 | -0.2 | 0.4 | -0.1 | -0.1 | -0.1 | -0.2 | -0.3 | -0.4 | -0.4 | 0 | -0.3 | 0.3 | -0.6 | 0.3 | 0.4 | 0.2 | 0.5 | 0.2 | 0 | -0.2 | 0.8 | 0.3 | 0 | -0.6 | 0 | 0.7 | -1.9 | -0.1 | 0.2 | 0 | -3.2 | 1.7 | 0 | 1.3 | -0.7 | 0.5 | -0.3 | 0.3 | 0 | -3.1 | -2.2 | At2g14750 | 266584_s_at | APK | adenylylsulfate kinase 1 (AKN1) / adenylylsulfate kinase 1, chloroplast precursor (APS kinase, Adenosine-5'phosphosulfate kinase, ATP adenosine-5'- phosphosulfate 3'-phosphotransferase) | 10 | Sulfur metabolism | Purine metabolism | Selenoamino acid metabolism | Biosynthesis of Amino Acids and Derivatives | Glutathione metabolism | 1.78 | 5.49 | |||||||||||||||||||||||||||
| AtCg00580 | 0.527 | PSBE | PSII cytochrome b559. There have been many speculations about the function of Cyt b559, but the most favoured at present is that it plays a protective role by acting as an electron acceptor or electron donor under conditions when electron flow through PSI | -0.7 | 0 | 0.2 | 0.7 | 0 | 0 | 0 | 0.1 | 0.1 | 0.1 | 0 | 0 | -0.6 | -0.2 | 0 | -0.6 | 0 | 0.2 | 0 | -0.1 | 0 | -0.6 | -0.4 | -0.4 | 0.5 | 0 | 0 | 0 | 0.3 | 0.6 | -0.1 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.2 | 0 | -0.4 | -0.3 | -0.3 | 0 | -0.2 | -0.1 | -0.2 | -0.3 | 0.1 | 0.1 | 0.2 | 0.3 | 0.1 | 0.3 | -0.1 | 0 | 0.1 | 0.3 | 0.1 | 0 | 0.1 | -0.1 | -0.2 | -0.2 | -0.3 | -0.3 | -0.2 | -0.2 | 0 | 0 | -0.4 | -0.3 | 0.6 | 0.5 | 0.3 | 0 | 0.4 | 0.1 | 0.1 | 0.1 | 0.3 | 0.5 | 0.5 | -0.2 | 0.1 | 0.4 | 0.4 | 0.4 | 0.5 | 0.2 | 0.2 | 0.1 | 0.2 | 0.5 | 0.2 | -0.3 | 0 | 0.1 | 0.2 | 0.1 | 0 | -0.1 | 0.1 | 0.1 | 0 | 0.1 | 0.1 | -0.1 | 0.1 | 0.5 | 0.5 | 0.5 | 0.2 | 0.1 | 0.1 | -0.3 | -0.1 | 0.3 | 0.4 | -0.1 | -0.8 | -0.4 | 0.2 | 0.7 | 0 | 0 | 0.5 | 0.2 | 0.2 | 0.2 | 0.1 | 0.6 | 0.1 | 0.5 | 0.3 | 0.2 | 0.5 | 0.1 | 0 | 0 | 0.1 | -0.1 | -0.5 | -0.5 | 0.4 | 0 | 0 | -0.1 | 0.1 | 0.5 | 0 | 0.6 | 0.4 | -0.1 | 0 | 0.5 | 0.9 | 0 | -1 | -0.3 | 0.2 | 0.5 | -1.2 | 0.1 | -0.6 | -0.4 | -0.2 | 0.4 | -0.3 | 0 | 0 | 0 | -0.6 | -0.6 | 0.3 | 0 | -0.1 | -0.6 | -0.4 | -0.1 | -0.1 | 0.2 | -0.3 | 0.3 | -0.4 | 0 | -0.1 | 0 | 0.1 | -0.6 | 0 | -0.2 | -0.3 | -0.9 | -0.4 | 0.2 | -0.2 | 0 | 0.1 | -0.1 | -0.3 | -2.1 | -5.7 | 1.8 | 0.2 | 0.8 | -0.8 | 0.2 | 0.5 | 0 | 0.4 | 0.2 | 0 | AtCg00580 | 244964_at | PSBE | PSII cytochrome b559. There have been many speculations about the function of Cyt b559, but the most favoured at present is that it plays a protective role by acting as an electron acceptor or electron donor under conditions when electron flow through PSI | 6 | oxygen evolving complex | electron transporter activity | heme binding | photosynthesis light harvesting in photosystem II | Photosystems | Photosystem II | Photosystem II reaction center | 1.24 | 7.60 | |||||||||||||||||||||||||||
| At1g31550 | 0.522 | GDSL-motif lipase family protein | -3.8 | 0 | 0 | 2.8 | -0.4 | -0.4 | -0.4 | -0.9 | 0.4 | -0.2 | 0 | 0.3 | 0.1 | -0.2 | 0.3 | 0.6 | -0.5 | -0.2 | 1 | -0.2 | -0.6 | -0.1 | 0.3 | 0 | 0.2 | 0.1 | -0.1 | 0 | 0.1 | 0.6 | 0.7 | 0.3 | 0.4 | -0.3 | -0.8 | -0.5 | -0.7 | -0.6 | 0 | 0.1 | 0.1 | 0.1 | 0.6 | 0.7 | 0.5 | 0 | 0.2 | 0.4 | -0.9 | 1.1 | -0.4 | -0.2 | 0 | -0.3 | -0.3 | -0.3 | -0.7 | 0 | -0.6 | -0.2 | -0.8 | 0.1 | -0.3 | -0.1 | 0.5 | 1.2 | 0.8 | 0.7 | 0 | 0.3 | 0 | 1.4 | 2 | 0 | 0 | 0 | 1.1 | 2.8 | 0 | 0 | 0 | 0.2 | -0.1 | 0 | 0 | 0.6 | 0 | 0 | 0 | 0 | -0.1 | -0.2 | 0 | 0.1 | 0.2 | 0.3 | 1.2 | 1.1 | 0 | 0 | 0 | 0 | -0.4 | 0 | 0.6 | -0.4 | -1.3 | -2.9 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | -0.1 | -0.6 | 0 | -0.2 | -0.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0.6 | -0.3 | 0.6 | 0.8 | 2.5 | 0.9 | 0.6 | 0.3 | 0 | 0.7 | 0.3 | 0 | 0 | 0 | 0 | -0.2 | -1 | 0 | 0.1 | 0 | -0.1 | -0.4 | -0.7 | -1.7 | -2.9 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.6 | 1.9 | -0.2 | 0 | -2.7 | -1 | 0.2 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.7 | 0 | 0 | 0 | 0.2 | 0 | -0.1 | 0 | 0.7 | 0.2 | 0.4 | 0.4 | 0.2 | -0.7 | -0.3 | 0.1 | 0 | -4.3 | 2.4 | 1.1 | 0.4 | -0.3 | 2.6 | 0 | -0.3 | 0 | -3.9 | 1.7 | At1g31550 | 256489_at | GDSL-motif lipase family protein | 2 | triacylglycerol degradation | 2.16 | 7.26 | ||||||||||||||||||||||||||||||
| At5g19220 | 0.520 | ADG2 | Biochemical studies of adg2-1 mutant indicate that mutant plants do not accumulate ADP glucose pyrophosphorylase (ADGase)large subunit protein and that ADGase small subunits assemble as homotetramers. ADG2 gene may encode the large subunit of ADGase. | Encodes the large subunit of ADP-glucose pyrophosphorylase which catalyzes the first, rate limiting step in starch biosynthesis. The large subunit plays a regulatory role whereas the small subunit (ApS) is the catalytic isoform. Four isoforms (ApL1-4) ha | -1.2 | 0.3 | 0.2 | 0.2 | 0 | -0.4 | -0.1 | -0.1 | -0.3 | -0.4 | 0 | 0.2 | -1.6 | -0.3 | -0.4 | -1.2 | 0 | 0.2 | -0.1 | 0 | -0.4 | -0.6 | 0.2 | 0 | -0.3 | -0.2 | 0 | 0.3 | -0.1 | -0.1 | -0.4 | -0.2 | 0 | 0 | -0.5 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.2 | 0 | -0.2 | -0.2 | -1.4 | 0.3 | 0 | -0.4 | -0.8 | -0.7 | 0.2 | 0.3 | 0 | 0.2 | 0 | 0.3 | -0.3 | 0.1 | -0.3 | 0 | -0.1 | 0.2 | 0 | 0.1 | 0.1 | 0 | -0.2 | -0.3 | 0 | 0.2 | 0.4 | 0.5 | 0.3 | 0.4 | 0.7 | 0.2 | 0.5 | -0.2 | 0 | 0.3 | 0.4 | 0.2 | 0.1 | 0.1 | 0.4 | 0.2 | 0.4 | 0.3 | 0.4 | 0.5 | 0.2 | 0.4 | 0.4 | 0.2 | 0 | -0.1 | 0.1 | 0.5 | 0.6 | 0 | 0.3 | 0.4 | 0 | 0.1 | 0 | -0.2 | -1.1 | -1.5 | 0 | 0 | 0 | 0 | 0 | -0.3 | 0.2 | 0.3 | 0.3 | -0.2 | -0.4 | -0.7 | 0 | 0.5 | 0.8 | 0.6 | 0.3 | 0.3 | 0 | 0.2 | 0.1 | 0.3 | 0.2 | 0 | 0 | 0.1 | 0 | 0.1 | 0.4 | 0.4 | -0.1 | -0.2 | 0 | 0 | -1.1 | 0 | 0.4 | 0.3 | -0.1 | 0.1 | 0.1 | 0.2 | -0.1 | 0 | 0.3 | -0.2 | 0.4 | 0.8 | 0.1 | 0.2 | 1.2 | 0.2 | 0.4 | 0.1 | 0.4 | -0.3 | -0.3 | -0.4 | 0.4 | 0.3 | 0.3 | 0.4 | 0.4 | 0.2 | 0.3 | 0.4 | 0.3 | 0.9 | -0.5 | -0.8 | -1.7 | -1.8 | -0.8 | -0.9 | -0.6 | -0.1 | 0.4 | 0.4 | 0.5 | 0.8 | 0.3 | 0.5 | 0.3 | 0.1 | 0 | 0.3 | 0 | -0.7 | -0.5 | -0.4 | 0 | 0.2 | 0 | -0.1 | -1.4 | -1.7 | -5.4 | 1.8 | 0.1 | 3.6 | 0.3 | 0.2 | 0.2 | -0.7 | 0.2 | -1.5 | 0.2 | At5g19220 | 249927_at | ADG2 | Biochemical studies of adg2-1 mutant indicate that mutant plants do not accumulate ADP glucose pyrophosphorylase (ADGase)large subunit protein and that ADGase small subunits assemble as homotetramers. ADG2 gene may encode the large subunit of ADGase. | Encodes the large subunit of ADP-glucose pyrophosphorylase which catalyzes the first, rate limiting step in starch biosynthesis. The large subunit plays a regulatory role whereas the small subunit (ApS) is the catalytic isoform. Four isoforms (ApL1-4) ha | 10 | C-compound, carbohydrate anabolism | starch biosynthesis | sucrose biosynthesis | trehalose biosynthesis III | colanic acid building blocks biosynthesis | dTDP-rhamnose biosynthesis | peptidoglycan biosynthesis | UDP-N-acetylglucosamine biosynthesis | galactose degradation I | glucose and glucose-1-phosphate degradation | UDP-glucose conversion | lactose degradation IV | sucrose degradation III | Starch and sucrose metabolism | Cell Wall Carbohydrate Metabolism | starch metabolism | 1.79 | 9.07 | |||||||||||||||||||||||||
| At4g30530 | 0.518 | strong similarity to defense-related protein (Brassica carinata) | -1.7 | 0 | 0 | -0.5 | 0.2 | 0.5 | 0 | 0 | 0.6 | 0.3 | 0 | 0.1 | 0.5 | -0.1 | 0.5 | 0.5 | 0 | 0.2 | 0 | 0.3 | 0.3 | -0.2 | 0.1 | 0 | 0 | -0.1 | 0 | 0.2 | 0 | 0.1 | 0.1 | 0 | 0.3 | -0.1 | -0.3 | -0.4 | -0.4 | -0.3 | -0.2 | -0.2 | -0.3 | -0.2 | 0 | 1.1 | 0.9 | 0 | -0.2 | 1.7 | 0.3 | 0.2 | 0.2 | -0.2 | 0 | 0 | 0 | 0.2 | 0.3 | 0.1 | 0.2 | 0.2 | -0.1 | -0.1 | -0.1 | 0 | 0.5 | 1.5 | 0.6 | 0.3 | 0 | 0.2 | 0 | 0.4 | 0.3 | -0.1 | 0 | 0.3 | 0.5 | 1 | 0 | 0 | 0 | -0.2 | 0.2 | 0.3 | 0.1 | 0 | -0.2 | 0 | -0.1 | -0.1 | -0.7 | -0.4 | -0.1 | -0.3 | -0.2 | -0.1 | 0.4 | 0.1 | -0.2 | 0 | 0.1 | 0.1 | -0.3 | 0 | 0.9 | 0.4 | -0.2 | 0.2 | 0 | 0 | -0.6 | -0.1 | -0.3 | 0.3 | 0 | -0.1 | 0 | 0.3 | -0.4 | 0 | 0 | 0.6 | 0.7 | 1.3 | 0 | -0.2 | 0.2 | -0.2 | 0.5 | 0.6 | 0.8 | 0.6 | 0.2 | 0 | -0.3 | 0.6 | 0.7 | 0.1 | 0.5 | 0.3 | 0.1 | 1.1 | -0.4 | 0.5 | -0.5 | 0 | -0.1 | -0.1 | -0.4 | -0.9 | -1.3 | -0.1 | -0.3 | -0.4 | -0.2 | -0.3 | -0.7 | 0.6 | 1.1 | 3 | 0 | -0.2 | -0.6 | -1.1 | -0.3 | -0.8 | -0.2 | 0 | 0 | -0.1 | -0.4 | -2.2 | -0.6 | -0.3 | -0.4 | 0.1 | -0.3 | -0.3 | -0.3 | -0.6 | -0.7 | -0.5 | -1 | -0.2 | -0.3 | 0.1 | -0.1 | -0.3 | 0 | 0.1 | 0.1 | 0.1 | 0 | 0 | 1 | 0.7 | 0 | -0.6 | -0.3 | -0.1 | -1.3 | 0.2 | 0.2 | 0.2 | -0.6 | 0 | -0.5 | 0.5 | 0 | 0.1 | -0.4 | -0.2 | 0 | -2 | -1.2 | At4g30530 | 253606_at | strong similarity to defense-related protein (Brassica carinata) | 2 | tryptophan biosynthesis | de novo biosynthesis of purine nucleotides I | de novo biosynthesis of purine nucleotides II | 1.64 | 5.24 | ||||||||||||||||||||||||||||||
| At2g20340 | 0.513 | tyrosine decarboxylase, putative, similar to tyrosine/dopa decarboxylase from Papaver somniferum and Tyrosine decarboxylase 3 from Petroselinum crispum | -4.2 | 0 | 0 | -0.1 | 0 | 0 | -0.4 | -0.4 | -0.2 | -0.8 | 0 | 0 | 1.9 | -0.1 | 1.4 | 0.2 | -0.4 | -1 | -0.2 | 0.2 | -0.9 | -1 | 0.3 | -0.3 | -0.3 | -0.4 | 0.1 | 0.5 | 0.1 | -0.2 | -0.2 | 0.3 | 0.1 | -0.1 | -1 | 0 | -0.2 | 0 | 0 | -0.1 | -0.5 | -0.8 | -0.5 | 0.1 | 0 | 0.2 | -0.2 | -0.8 | -0.8 | -0.4 | 0 | -0.1 | 0 | -0.2 | 0 | -0.1 | -0.7 | 0.2 | -0.6 | -0.1 | -0.6 | 0.1 | -0.1 | -0.2 | 0.2 | 1.2 | 0.3 | -0.2 | -0.6 | -0.2 | 0 | 0.1 | 0.1 | 0.2 | 0.1 | -0.8 | -0.3 | -0.1 | 0.1 | 0.2 | 0.1 | 0.2 | -0.2 | 0 | 0.1 | 0 | 0 | -0.1 | 0 | 0.5 | 0.2 | 0.1 | 0.3 | 0.4 | 0.3 | 0.5 | 0 | 0.1 | 0 | 0.4 | 0 | 0.2 | 0 | 0.4 | 0.7 | 0.4 | -0.6 | 0 | 0.1 | 0 | 0.9 | 1.4 | 1.2 | 1.3 | 0.3 | 0.5 | 0.3 | 0.4 | -0.1 | 0.3 | 0 | 0.2 | 0.2 | 0.9 | 0.8 | 0.9 | 0.5 | -0.1 | 1.1 | 1.5 | 2.1 | 0.3 | 0 | 0.3 | -0.5 | 0.3 | 0 | 0.9 | 0.8 | 0.7 | 0.1 | 0.1 | -0.6 | 0 | 0 | 0.1 | 0.6 | 0 | -0.2 | -1.6 | -1 | 0.2 | 0 | 0.3 | 0.8 | -0.5 | -1.2 | 0 | 0.9 | 0 | 0 | 0 | 0 | -0.9 | -0.7 | -0.1 | -0.2 | 0 | -0.2 | 0 | 0 | -0.7 | -1.3 | -0.1 | -0.3 | -0.4 | -0.2 | -0.3 | 0.4 | 0.4 | 0 | 0.2 | 0 | 0.3 | -0.2 | 0.9 | 0.1 | -0.1 | -0.3 | -0.6 | -0.6 | -0.3 | 0.1 | 0.6 | -0.5 | -0.9 | -0.7 | -0.2 | 0.6 | 0.4 | -0.4 | 0.2 | 0 | -0.4 | -1.4 | 1.1 | -0.5 | 0.8 | 0.3 | 0.4 | 0 | -0.1 | 0 | -1.9 | 0 | At2g20340 | 265305_at | tyrosine decarboxylase, putative, similar to tyrosine/dopa decarboxylase from Papaver somniferum and Tyrosine decarboxylase 3 from Petroselinum crispum | 4 | Tyrosine metabolism | Alkaloid biosynthesis I | 1.89 | 6.40 | ||||||||||||||||||||||||||||||
| At1g44575 | 0.506 | NPQ4 | Encoding PSII-S (CP22), a ubiquitous pigment-binding protein associated with photosystem II (PSII) of higher plants. Involved in nonphotochemical quenching rather than in photosynthesis. | -2.8 | 0.1 | 0.1 | 0.3 | 0 | -0.2 | 0.1 | -0.1 | -1.5 | -0.8 | -0.1 | 0 | -1.9 | -0.2 | -0.2 | -0.8 | 0.1 | 0 | -0.6 | 0 | -0.3 | -0.8 | 0 | 0 | -0.3 | -0.3 | 0 | 0 | 0 | -0.2 | -0.4 | -0.1 | 0.1 | -0.1 | -0.2 | 0 | 0.1 | 0.1 | 0.1 | 0 | 0 | 0.1 | -0.2 | -0.2 | -1.4 | 0.1 | -0.1 | -0.3 | -0.1 | -0.7 | 0.2 | 0.1 | 0 | 0.1 | -0.1 | 0.2 | -0.5 | 0.2 | -0.4 | 0.1 | -0.3 | 0.1 | -0.1 | 0.2 | 0 | 0 | -0.2 | -0.1 | 0 | 0 | 0.4 | 0.3 | 0.1 | 0.3 | 0.6 | 0 | 0.4 | -0.2 | 0.1 | 0 | 0.3 | 0.2 | 0.2 | 0.1 | 0 | 0.1 | -0.1 | -0.2 | 0.3 | 0.1 | 0.1 | 0.2 | 0.2 | 0.3 | 0 | 0 | 0 | 0.2 | 0.1 | 0.3 | 0.2 | 0.5 | 0 | 0 | 0 | -0.4 | -1.6 | -1.1 | 0.2 | 0.3 | 0 | 0.1 | 0.7 | 0.5 | 0.1 | 0.2 | 0.1 | -0.1 | -0.3 | 0 | 0.1 | 0.2 | -0.1 | 0.3 | 0.6 | 0.9 | -0.1 | 0.6 | 0.2 | 0.2 | 0.2 | 0.1 | 0 | 0.2 | 0.2 | 0 | 0.5 | 0 | 0.1 | 0 | -0.1 | 0 | -0.6 | -0.1 | 0 | 0 | 0.3 | 0.3 | 0.6 | 0 | -0.2 | 0.6 | 0.6 | 0.5 | 0.6 | 0 | 0.1 | 0 | 0.6 | 0.3 | 0.4 | 0 | 0 | 0 | 0 | -0.2 | -0.1 | 0 | 0.4 | 0.1 | 0.1 | 0 | 0 | 0.1 | 0.3 | 0 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.9 | 0.8 | 0.6 | -0.1 | 0.3 | 0.2 | 0.4 | 0 | 0.3 | 0.2 | -0.2 | -0.2 | -0.2 | 0 | 0 | 0 | 0 | -0.4 | -3.2 | -5.9 | 1.7 | 0.3 | 1.2 | 0.2 | -0.2 | 0.1 | -0.3 | -0.3 | 0 | 1.9 | At1g44575 | 245213_at | NPQ4 | Encoding PSII-S (CP22), a ubiquitous pigment-binding protein associated with photosystem II (PSII) of higher plants. Involved in nonphotochemical quenching rather than in photosynthesis. | 8 | nonphotochemical quenching | PSII associated light-harvesting complex II | chlorophyll binding | Photosynthesis | Photosystems | Photosystem II | 1.42 | 7.91 | ||||||||||||||||||||||||||
| At2g38540 | 0.506 | LTP1 | non-specific lipid transfer protein. specifically expressed in L1 epidermal layer. | -2.3 | 0.1 | -1.2 | 0.1 | 0 | 0 | 0.3 | 0.2 | -0.5 | 0 | 0 | 0 | -1.6 | -0.1 | 0 | -0.9 | -0.1 | -0.3 | -0.9 | 0 | -0.6 | -1.8 | 0 | 0.1 | -0.3 | -0.2 | -0.1 | 0 | 0 | -0.2 | -0.5 | -0.5 | 0.1 | 0 | -0.4 | -0.2 | 0.1 | 0.2 | 0 | 0 | 0 | -0.3 | -0.9 | 0 | -1.3 | 0 | 0.5 | -0.7 | -0.9 | -0.3 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | -0.5 | -0.1 | -0.6 | -0.3 | -0.2 | 0 | 0 | 0.1 | 0.1 | 0 | 0.3 | 0 | 0.1 | 0.1 | -1 | 0.2 | 1.3 | -0.5 | 0 | -1.3 | 0.3 | -0.2 | 0.4 | 0.1 | 0 | -0.2 | 0.1 | 0 | 0.4 | 1.7 | -1.1 | 0 | 0.2 | 0.6 | 0.3 | 0 | 0.1 | -0.1 | -0.1 | 0 | 0.3 | 1.4 | -1.1 | 0.6 | -0.1 | 0.3 | 0.1 | 0.2 | 0.3 | 0.4 | 0.9 | 0.7 | -0.1 | 0.9 | 1.1 | 3.3 | 2.5 | 2.1 | 0.4 | 0.3 | 0.4 | 0.6 | 0.8 | 0.8 | 0 | 1.2 | 0 | 0.5 | 2 | 0.2 | 0 | 0.1 | 0.5 | 0.1 | 0.2 | 0 | 0.3 | 0.3 | -0.7 | -0.4 | 1.6 | -0.3 | 0.9 | -0.3 | 0.2 | 0.1 | 0.3 | 0 | 0.2 | 0.3 | 0.3 | 0 | -0.1 | 0.1 | 0.2 | -0.4 | 0.5 | 0 | 0.3 | 0 | 0.3 | 0 | 0.1 | 0.1 | 0.1 | 0.4 | 0.2 | 0.3 | 0 | -0.3 | 0 | 0 | -0.6 | 0.3 | 0.2 | -1.2 | 0.3 | 0.6 | -1.1 | 0 | 0 | -0.1 | -0.2 | -0.6 | -0.3 | -0.6 | -0.4 | -0.5 | -1.1 | 0 | 0.9 | -1.7 | -0.2 | -0.2 | -0.5 | 0 | 0.1 | 0 | -0.6 | -0.9 | 0 | -0.2 | 0.1 | -0.1 | 0 | 0 | 0.9 | 0.1 | -7.6 | 2.3 | 0.7 | 1 | -0.1 | -0.3 | 0.9 | 0 | 0.1 | -1 | 0.1 | At2g38540 | 266421_at | LTP1 | non-specific lipid transfer protein. specifically expressed in L1 epidermal layer. | 2 | lipid transport | Miscellaneous acyl lipid metabolism | 2.24 | 11.00 | |||||||||||||||||||||||||||
| At1g78680 | 0.503 | GGH1 | gamma-glutamyl hydrolase (GGH1) / gamma-Glu-X carboxypeptidase / conjugase | -1.8 | 0 | -0.1 | -0.5 | -0.3 | -0.6 | -0.6 | -0.9 | -0.5 | -0.5 | 0 | 0 | 0.1 | -0.3 | -0.1 | 0 | -0.5 | -0.5 | 0 | 0 | -0.8 | -0.9 | 0.1 | -0.3 | -0.6 | -0.4 | -0.2 | 0.1 | -0.1 | -0.2 | -0.2 | 0.2 | -0.2 | -0.1 | -0.5 | -0.5 | -0.3 | -0.1 | -0.1 | -0.3 | -0.6 | -1 | -1.1 | 0 | -0.2 | -0.2 | -0.5 | -0.9 | -1.1 | 0 | -0.2 | -0.1 | 0 | -0.3 | -0.3 | 0 | -1.1 | 0 | -1 | -0.2 | -0.8 | 0.1 | -0.3 | 0.2 | -0.1 | 0.3 | 0.2 | -0.1 | -0.2 | -0.2 | 0.6 | 0.1 | 0.1 | 0.3 | 0.7 | 0.6 | 0.2 | -0.8 | 0.1 | 0 | 0.7 | 0.3 | 0.3 | 0.4 | 0.1 | 0 | 0.1 | 0 | 0 | 0.5 | 0.3 | 0 | 0.4 | 0.4 | 0.6 | 0.2 | 0 | 0.2 | 0.3 | 0.2 | 0.2 | 0.2 | 0 | 0.2 | 1.6 | 1.1 | 0.6 | 1.2 | 0 | 0.9 | 1.4 | 1.1 | 1.3 | 1.2 | 0 | 0.4 | 1.8 | 1.2 | 1.3 | 1.1 | 0.2 | 0.6 | 0.7 | 0.3 | 1.2 | 0.6 | 0.2 | 0 | 1.3 | 0.9 | 1.4 | 0.7 | 0.2 | 0.4 | 0 | -0.1 | 0 | 0.2 | 0 | 0 | 0 | -0.5 | 0.7 | -0.3 | -0.4 | 0.4 | -0.4 | -1.3 | -1.5 | -1.6 | -1.5 | -0.2 | -0.2 | -0.1 | -0.2 | -0.4 | -0.7 | -0.1 | 0.6 | -0.5 | 0.5 | 0.6 | 0 | -0.7 | -0.1 | -0.1 | -0.1 | 0.2 | 0.4 | 0 | 0.1 | 0.4 | 1.1 | 0.6 | 1 | 0.4 | -0.3 | -0.4 | -1.2 | 0.5 | 0.5 | 0.3 | 0 | 0 | 0 | -0.1 | 0.2 | 0.1 | 0.2 | 0.4 | 0.2 | 0 | 0.2 | -0.7 | -1.2 | -1.3 | -0.8 | -0.9 | 0.7 | 0.6 | -0.3 | -0.4 | 0.3 | -1.3 | -2.8 | 2 | 0.7 | 0.5 | 0.2 | -0.1 | 0 | -0.3 | 0 | -2.4 | 0 | At1g78680 | 264250_at | GGH1 | gamma-glutamyl hydrolase (GGH1) / gamma-Glu-X carboxypeptidase / conjugase | 6 | Folate biosynthesis | 2.39 | 4.88 | ||||||||||||||||||||||||||||
| At4g12800 | 0.501 | photosystem I reaction center subunit XI, chloroplast (PSI-L) / PSI subunit V | -1.2 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | -1 | -0.5 | -0.3 | 0 | -1.4 | -0.4 | -0.3 | -0.6 | 0 | 0 | -0.4 | -0.1 | -0.3 | -0.6 | 0 | 0 | -0.2 | -0.1 | -0.1 | 0 | 0 | 0 | -0.2 | -0.2 | 0.2 | -0.2 | -0.2 | 0 | 0.1 | 0 | 0 | 0.1 | 0 | 0 | -0.2 | -0.2 | -0.6 | 0 | 0 | 0 | -0.1 | -0.5 | 0 | 0 | 0 | 0.1 | -0.2 | 0.1 | -0.3 | 0.1 | -0.4 | 0 | -0.3 | 0 | -0.1 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0.2 | 0.4 | 0.5 | 0.4 | 0.6 | 1.2 | -0.5 | 0.5 | -0.3 | 0 | 0 | 0 | -0.3 | 0 | -0.2 | 0.1 | 0.3 | 0.1 | 0 | 0.4 | 0 | 0.1 | 0 | 0 | -0.3 | 0 | 0 | 0.5 | 0.6 | 0.6 | 0.9 | 0.2 | 0.8 | 0 | 0 | -0.1 | -0.3 | -0.4 | -0.6 | -0.3 | -0.3 | 0 | 0.8 | 0.9 | 1 | 0 | 0.1 | 0.2 | -0.2 | -0.1 | -0.3 | 0.2 | 0.1 | 0.1 | 0.5 | 1.1 | 1.3 | -0.2 | 0.2 | 0 | -0.3 | -0.2 | -0.2 | 0 | 0.2 | 0.3 | -0.2 | 0.3 | 0.1 | 0.8 | -0.2 | 0 | 0 | 0.2 | -0.3 | -0.3 | -0.1 | 0 | 0 | -0.2 | 0.3 | -0.1 | 0.6 | 1.1 | 1.3 | 1.4 | 0.3 | -0.4 | 0.2 | 0.7 | -0.1 | 0 | 0 | 0.1 | 0 | -0.3 | -0.4 | -0.2 | 0 | 0 | 0 | -0.4 | -0.1 | 0.1 | 0.2 | -0.8 | -0.7 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.3 | 1 | 0.1 | 0.6 | 0.4 | 0.2 | 0.3 | 0.1 | -0.2 | 0 | -0.2 | -0.7 | -0.1 | 0 | -0.3 | -0.1 | 0 | -0.2 | 0 | -2.5 | -6.7 | 2 | -0.2 | 1.2 | 0 | -0.3 | 1.5 | -0.1 | -0.1 | -0.3 | 2.9 | At4g12800 | 254790_at | photosystem I reaction center subunit XI, chloroplast (PSI-L) / PSI subunit V | 4 | photosynthesis | accessory proteins of photosynthetic electron transport | Photosynthesis | Photosystems | Photosystem I | photosystem I subunit precursor | 1.66 | 9.66 | ||||||||||||||||||||||||||||
| page created by Juergen Ehlting | 04/20/06 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||