Co-Expression Analysis of: | CYP71B26 (At3g26290) | 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 | |||||||||||||||||||||
At3g26290 | 1.000 | CYP71B26 | cytochrome P450 family protein | -5.43 | 0.46 | 0.41 | -1.58 | -0.99 | -1.32 | -0.49 | -0.95 | -0.31 | -0.21 | 0.14 | 0.19 | 0.86 | -0.46 | -0.61 | 0.35 | 0.09 | 0.01 | 0.1 | 0.03 | -0.74 | 0.18 | 0.64 | 0.26 | -0.28 | -0.14 | -0.33 | 1.43 | -0.25 | -0.37 | -0.33 | -0.08 | 0.07 | -0.34 | -0.93 | -0.07 | -0.07 | 0.05 | 0.04 | 0.18 | -0.33 | -0.42 | -0.16 | 0.4 | 0.69 | -0.11 | -0.93 | -0.11 | 1.85 | 0.69 | -0.63 | 0.24 | 0.16 | -0.4 | 0.19 | -0.35 | -0.57 | 0 | -0.4 | -0.72 | 0.16 | 0.57 | 0.22 | 0.2 | -0.73 | -0.78 | 0.03 | 0.16 | 0.77 | 0.39 | 0.06 | 0.01 | 0.48 | 0.05 | -0.15 | 0.56 | 0.19 | 0.62 | -0.44 | -0.12 | -0.15 | 0.1 | 0.14 | 0.03 | -0.05 | 0.46 | -0.24 | 0.07 | 0.12 | 0.2 | -0.46 | -0.08 | -0.15 | 0.14 | 0.54 | 0.09 | 0.02 | 0.32 | -0.59 | -0.48 | 0.2 | 0.28 | -0.15 | -0.02 | 1.07 | 1.73 | 2.4 | 2.39 | -0.64 | -0.22 | 0.16 | -0.15 | 0.22 | 0.49 | -0.12 | 0.04 | 1.2 | 1.42 | 1.95 | 1.41 | -0.34 | 0.12 | -0.82 | -0.79 | 0.38 | 0.46 | 0.25 | 0.44 | 0.73 | -0.45 | 0.16 | 0.14 | 0.4 | 0.26 | -0.45 | -0.7 | -0.26 | -0.14 | -0.73 | -0.13 | -0.34 | -1.42 | -0.28 | -0.08 | 1.8 | -0.1 | -1.33 | -1.43 | -1.2 | 1.23 | -0.5 | 0.05 | 0.34 | -0.68 | 0.01 | 0.65 | -2.35 | -1.44 | 0.54 | 0.02 | 0.7 | 0.4 | -0.43 | -0.55 | -0.32 | -0.25 | -0.59 | 0.1 | 0.24 | 0.28 | 0.24 | -0.67 | 0.22 | -0.1 | -0.1 | 0.09 | 0.02 | 0.02 | 0.07 | 0.02 | 0.02 | 0.02 | 0.02 | 0.02 | -0.17 | 0.07 | 1.02 | -1.02 | -0.07 | 0.46 | 0.04 | 0.55 | 1.04 | -0.82 | -1.03 | 0.24 | 1.23 | -0.09 | -0.11 | 0.24 | -1.07 | 0.51 | 1.49 | -0.51 | -5.87 | 5.46 | 3.55 | 0.02 | -0.07 | 0.15 | 0.03 | 0.4 | 0.02 | -1.45 | 0.02 | At3g26290 | 257628_at | CYP71B26 | cytochrome P450 family protein | 1 | cytochrome P450 family | 2.52 | 11.34 | ||||||||||||||||||||||||||||
At3g61990 | 0.652 | O-methyltransferase family 3 protein | -0.11 | -0.12 | -0.02 | -0.26 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | 0.68 | -0.12 | -0.12 | 0.69 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.04 | -0.12 | -0.12 | -0.12 | 0.06 | -0.12 | -0.57 | 0.13 | -0.24 | 0.51 | 1 | -0.12 | -0.12 | -0.12 | 1.08 | 2.25 | -0.44 | -0.12 | -0.12 | -0.12 | 0.21 | -0.12 | -0.12 | -0.12 | -0.18 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | 0.08 | -0.12 | 0.5 | 0.41 | 1.29 | 0.77 | -0.22 | -0.06 | 0.33 | 0.08 | 0.46 | -0.32 | 0.02 | -0.05 | -0.12 | 0.12 | 0.09 | 0.01 | 0.28 | -0.12 | 0.02 | 0.59 | -0.3 | -0.1 | -0.04 | -0.03 | -0.12 | 0.02 | -0.12 | -0.12 | 1.26 | 0.12 | 0.01 | 0.48 | -0.49 | 0.16 | -0.04 | 0.45 | -0.12 | -0.12 | 0.2 | 1.33 | 3.15 | 3.05 | -0.33 | -0.08 | -0.65 | -0.05 | -0.2 | -0.45 | -0.12 | -0.12 | 0.28 | 0.82 | 1.23 | 0.3 | -0.16 | 0.24 | -0.87 | -1.57 | -0.62 | -0.8 | 0.13 | -0.12 | 0.31 | 0.16 | 0.14 | 0.32 | 1.24 | 0.7 | -0.15 | -0.3 | 0.2 | -0.13 | 0.66 | 0.38 | 0.02 | -0.7 | 0.53 | -0.14 | -0.68 | -0.12 | -0.12 | -0.12 | -0.12 | -0.12 | -0.77 | -0.21 | 0.09 | -0.11 | 0.06 | -0.3 | -1.29 | -0.48 | -2.06 | -0.72 | -0.12 | -0.12 | -0.12 | -0.12 | -0.53 | -0.12 | 0.91 | 0.32 | -0.04 | 0.1 | 0.04 | -0.54 | -0.81 | -0.33 | -0.03 | 0.03 | -0.2 | -0.7 | -1.12 | -0.65 | -0.48 | -0.18 | -0.03 | -0.24 | -0.62 | 0.12 | 0.37 | -0.85 | 0.11 | 0.36 | -0.48 | 0.36 | 0.23 | -0.12 | -0.12 | 0.54 | 1.08 | -0.75 | -0.12 | -0.12 | -0.12 | 1.18 | 0.18 | -0.39 | -5.74 | 4.98 | 0.84 | -1.79 | -0.39 | 0.45 | 0.28 | -0.23 | -0.11 | 0.09 | 0.88 | At3g61990 | 251304_at | O-methyltransferase family 3 protein | 2 | secondary metabolism | Phenylpropanoid pathway | Methyltransferase, CCOMT like | 1.84 | 10.72 | ||||||||||||||||||||||||||||
At4g39210 | 0.632 | APL3 | 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) hav | -2.04 | -0.3 | -0.07 | -0.23 | -0.15 | -1.44 | -0.25 | -0.44 | -1.36 | -0.56 | -0.28 | -0.55 | -0.59 | -0.48 | -0.02 | -0.56 | -0.62 | -0.36 | -0.23 | -0.4 | -0.43 | -0.39 | 0 | -0.39 | -0.02 | -0.01 | -0.31 | 0.13 | -0.5 | -0.08 | -0.41 | -0.36 | 0.46 | -0.3 | -0.82 | -0.7 | -0.71 | -0.6 | -0.4 | -0.2 | -0.78 | -0.28 | -0.01 | 0.26 | -0.01 | 0.06 | 0.42 | -0.48 | 0.24 | 0.79 | -0.74 | -0.39 | -0.16 | -0.79 | -0.38 | -0.83 | -1.57 | -0.47 | -1.38 | -0.68 | -1.1 | -0.46 | -0.4 | -0.08 | -0.28 | -0.53 | -0.04 | -0.21 | -0.43 | -0.66 | -0.6 | 0.17 | 0.02 | -0.09 | -0.16 | -0.87 | 0.16 | -0.13 | 0.12 | -0.3 | -0.04 | -0.3 | -0.1 | 0.14 | 0.2 | 0.3 | 0.06 | -0.3 | -0.49 | 0.11 | -0.53 | -0.03 | -0.02 | -0.37 | 0.68 | 0.56 | -0.05 | 0.16 | 0.34 | 0.35 | 0.11 | 0.84 | -0.15 | -0.09 | 1.98 | 2.21 | 3.32 | 2.83 | 0.02 | 0.06 | 0.08 | 0.3 | 0.15 | 1.19 | -0.14 | 0.01 | 1.94 | 2.34 | 3.47 | 3.5 | -0.1 | 0.06 | 0.19 | 1.04 | 1.56 | 2.82 | 0.48 | 0.3 | 0.45 | 0.34 | 0.78 | -0.01 | -0.06 | -0.28 | -0.28 | -0.15 | 0.25 | -0.11 | 0.16 | -0.1 | 0.44 | -0.49 | -2.02 | 1.05 | 4.34 | 0.07 | -1.03 | -0.47 | -0.38 | -0.72 | -0.17 | 0.12 | 0.22 | 0.03 | -0.11 | -0.73 | 0.01 | -0.07 | 2.17 | 0.61 | 0.6 | 0.03 | -0.95 | -1.8 | -0.53 | 0.16 | 0.88 | 0.14 | -0.03 | -0.13 | 0.08 | 0.06 | -0.28 | 0.48 | -0.13 | 0.36 | -0.16 | -0.67 | -0.63 | -1.13 | -0.31 | 0.27 | -0.43 | 0.09 | -0.32 | 0.36 | 0.21 | -0.21 | -0.1 | -0.4 | 0.02 | 0.21 | -0.09 | -0.65 | -1.23 | -0.97 | 0.96 | -0.38 | 0.6 | -0.1 | -0.83 | 0.9 | 1.24 | -0.66 | -3.87 | 2.79 | 0.8 | 1.81 | -0.3 | 1.1 | -0.07 | 0.28 | -0.07 | -2.15 | 0.36 | At4g39210 | 252888_at | APL3 | 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) hav | 10 | starch biosynthesis | C-compound and carbohydrate utilization | starch biosynthesis | Starch and sucrose metabolism | Cell Wall Carbohydrate Metabolism | starch metabolism | 3.06 | 8.20 | ||||||||||||||||||||||||
At3g44300 | 0.624 | 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 | 0.04 | 0.17 | -0.56 | -0.31 | -0.35 | -0.28 | -0.19 | 0.15 | 0.07 | -0.24 | -0.14 | 0.22 | -0.04 | 0.14 | 0.28 | 0 | -0.14 | -0.08 | -0.12 | -0.12 | -0.24 | 0.05 | 0.13 | -0.05 | -0.02 | -0.06 | 0.04 | 0.02 | 0.03 | -0.12 | 0.18 | 0 | -0.35 | -0.28 | -0.19 | -0.23 | -0.09 | -0.2 | -0.16 | -0.46 | -0.35 | -0.42 | 0.57 | 1.06 | -0.19 | -0.13 | 0.4 | -0.28 | -0.27 | -0.2 | -0.06 | 0.03 | -0.03 | -0.19 | -0.03 | -0.28 | -0.06 | -0.27 | -0.15 | -0.4 | 0.11 | -0.13 | 0.18 | -0.3 | 0.13 | 0.32 | -0.19 | 0.15 | 0.12 | -0.55 | 0.16 | 0.24 | 0.06 | 0.62 | -0.43 | 0.31 | 0.11 | -0.08 | 0.06 | 0.05 | -0.18 | -0.2 | 0.16 | 0.12 | 0.57 | -0.36 | 0.15 | 0.23 | 0.46 | -0.31 | -0.1 | 0.03 | -0.06 | -0.1 | -0.02 | 0.01 | 0.45 | -0.65 | 0.01 | -0.1 | 0.11 | -0.06 | -0.19 | -0.12 | -0.27 | -0.45 | 0.25 | -0.24 | 0.28 | 0.43 | 1.25 | 1.15 | 1.31 | -0.14 | -0.09 | 0.06 | 0.28 | 0.01 | 0.45 | -0.15 | 0.27 | 0.52 | 0.89 | 0.98 | 1.26 | 0.11 | 0.23 | -0.04 | -0.2 | 0.36 | 0.2 | 0.13 | 0.11 | -0.48 | -0.18 | -0.01 | 0.07 | 0.84 | 0.1 | 0.15 | -0.1 | 0.85 | -0.03 | -0.62 | 0.12 | -0.19 | 0.14 | -0.02 | -0.56 | -1.12 | -0.12 | 0.26 | -0.38 | 0.23 | -0.23 | -0.28 | -0.5 | 0.19 | -0.27 | 0.21 | -0.1 | -0.27 | -0.22 | -0.14 | -0.28 | -0.33 | 0 | -0.28 | 0.07 | -0.03 | -0.81 | -0.24 | 0.17 | 0.32 | 0.08 | 0.03 | 0.14 | -0.01 | -0.39 | -0.38 | -0.39 | -0.39 | -0.39 | -0.48 | 0.27 | 0.5 | -0.39 | -0.17 | -0.2 | -0.05 | 0.2 | -0.07 | -0.45 | -0.52 | -0.4 | -0.34 | -0.25 | -0.73 | -0.12 | -0.52 | 0.11 | 0.7 | 0.16 | -6.74 | 6.48 | 4.34 | -0.02 | -0.02 | -0.06 | 0.76 | 0.24 | -0.39 | -1 | -0.02 | 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 | 0.624 | 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 | 0.04 | 0.17 | -0.56 | -0.31 | -0.35 | -0.28 | -0.19 | 0.15 | 0.07 | -0.24 | -0.14 | 0.22 | -0.04 | 0.14 | 0.28 | 0 | -0.14 | -0.08 | -0.12 | -0.12 | -0.24 | 0.05 | 0.13 | -0.05 | -0.02 | -0.06 | 0.04 | 0.02 | 0.03 | -0.12 | 0.18 | 0 | -0.35 | -0.28 | -0.19 | -0.23 | -0.09 | -0.2 | -0.16 | -0.46 | -0.35 | -0.42 | 0.57 | 1.06 | -0.19 | -0.13 | 0.4 | -0.28 | -0.27 | -0.2 | -0.06 | 0.03 | -0.03 | -0.19 | -0.03 | -0.28 | -0.06 | -0.27 | -0.15 | -0.4 | 0.11 | -0.13 | 0.18 | -0.3 | 0.13 | 0.32 | -0.19 | 0.15 | 0.12 | -0.55 | 0.16 | 0.24 | 0.06 | 0.62 | -0.43 | 0.31 | 0.11 | -0.08 | 0.06 | 0.05 | -0.18 | -0.2 | 0.16 | 0.12 | 0.57 | -0.36 | 0.15 | 0.23 | 0.46 | -0.31 | -0.1 | 0.03 | -0.06 | -0.1 | -0.02 | 0.01 | 0.45 | -0.65 | 0.01 | -0.1 | 0.11 | -0.06 | -0.19 | -0.12 | -0.27 | -0.45 | 0.25 | -0.24 | 0.28 | 0.43 | 1.25 | 1.15 | 1.31 | -0.14 | -0.09 | 0.06 | 0.28 | 0.01 | 0.45 | -0.15 | 0.27 | 0.52 | 0.89 | 0.98 | 1.26 | 0.11 | 0.23 | -0.04 | -0.2 | 0.36 | 0.2 | 0.13 | 0.11 | -0.48 | -0.18 | -0.01 | 0.07 | 0.84 | 0.1 | 0.15 | -0.1 | 0.85 | -0.03 | -0.62 | 0.12 | -0.19 | 0.14 | -0.02 | -0.56 | -1.12 | -0.12 | 0.26 | -0.38 | 0.23 | -0.23 | -0.28 | -0.5 | 0.19 | -0.27 | 0.21 | -0.1 | -0.27 | -0.22 | -0.14 | -0.28 | -0.33 | 0 | -0.28 | 0.07 | -0.03 | -0.81 | -0.24 | 0.17 | 0.32 | 0.08 | 0.03 | 0.14 | -0.01 | -0.39 | -0.38 | -0.39 | -0.39 | -0.39 | -0.48 | 0.27 | 0.5 | -0.39 | -0.17 | -0.2 | -0.05 | 0.2 | -0.07 | -0.45 | -0.52 | -0.4 | -0.34 | -0.25 | -0.73 | -0.12 | -0.52 | 0.11 | 0.7 | 0.16 | -6.74 | 6.48 | 4.34 | -0.02 | -0.02 | -0.06 | 0.76 | 0.24 | -0.39 | -1 | -0.02 | 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 | ||||||||||||||||||||||||||
At4g03050 | 0.603 | 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 | 0.12 | 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 | 0.08 | 0 | -0.42 | 0 | 0 | 0 | 0 | 0 | 0.19 | -0.12 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.45 | 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 | -0.85 | 0 | 0 | -8.47 | 8.16 | 2.87 | 0 | 0 | 0 | -1.12 | 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 | |||||||||||||||||||||||||
At5g36160 | 0.602 | aminotransferase-related, similar to nicotianamine aminotransferase B (Hordeum vulgare subsp. vulgare) | -1.06 | 0.18 | 0.19 | -0.23 | -0.51 | -0.95 | -0.52 | -0.33 | -0.1 | -0.09 | 0.38 | -0.28 | 0.85 | 0.13 | -0.45 | 0.09 | 0.17 | -0.25 | 0.01 | -0.1 | -1 | -0.11 | 0.17 | -0.1 | -0.01 | -0.03 | -0.52 | 0.37 | -0.18 | 0 | -0.09 | -0.11 | -0.17 | 0.14 | 0.08 | -0.15 | -0.16 | -0.09 | -0.19 | -0.23 | -0.68 | -0.61 | -0.49 | 0.39 | 0.68 | -0.31 | 0.51 | 0 | 0.16 | 0.21 | -0.26 | -0.01 | 0.19 | -0.23 | 0.03 | -0.31 | -1.03 | -0.27 | -0.88 | -0.42 | -0.66 | -0.03 | 0.09 | 0.35 | -0.25 | 0.23 | 1.08 | 0.3 | 0.08 | 0.49 | -0.26 | 0.19 | -0.11 | 0.22 | 0.21 | -0.21 | 0 | 0.22 | -0.08 | 0.05 | -0.05 | 0.01 | -0.36 | -0.2 | 0.05 | 0.27 | -0.24 | 0.03 | 0.17 | 0.18 | -0.28 | -0.23 | 0.11 | -0.03 | -0.27 | 0.2 | -0.05 | 0.05 | -0.05 | 0.25 | 0.47 | 0.66 | 0.34 | -0.04 | 0.76 | 1.7 | 0.71 | 0.84 | -0.3 | -0.09 | -0.23 | 0.28 | 0.26 | 0.08 | -0.02 | -0.25 | 0.55 | 1.33 | 0.52 | 0.83 | -0.13 | -0.26 | -0.45 | -0.77 | 0.2 | 0.44 | 0.24 | 0.28 | 0.08 | 0.06 | 0.68 | 0.36 | 0.05 | -0.16 | -0.43 | -0.41 | -0.48 | -0.17 | 0.25 | 0.14 | -0.09 | 0.03 | -0.03 | 0.63 | 1.17 | 0.15 | 0.13 | 0.33 | 0.49 | -0.55 | -1.11 | 0.14 | 0.05 | 0.14 | 0.05 | -0.44 | -1.55 | -0.59 | -0.15 | 0.21 | 0.44 | -0.2 | -0.6 | -0.99 | -0.48 | 0.52 | -0.11 | 0.23 | 0.15 | 0.02 | -0.2 | -0.87 | -0.1 | 0.57 | 0.41 | 0.46 | -0.22 | -0.5 | -0.75 | -1.18 | -0.66 | -0.22 | 0.2 | -0.06 | -0.02 | 0.31 | 0.09 | -0.14 | 0.37 | 0.04 | 0.11 | 0.48 | 0.49 | -0.32 | -0.17 | 0.62 | -0.01 | -0.07 | 0.14 | 0.22 | -0.46 | -0.09 | 1.01 | 0.21 | -2.8 | 0.81 | 0.54 | 1.73 | -0.24 | 0.39 | 0.02 | 0.64 | -0.08 | -0.28 | 0.76 | At5g36160 | 249688_at | aminotransferase-related, similar to nicotianamine aminotransferase B (Hordeum vulgare subsp. vulgare) | 2 | nitrogen and sulfur utilization | phenylalanine biosynthesis II | phenylalanine degradation I | tyrosine degradation | 1.56 | 4.53 | |||||||||||||||||||||||||||||
At2g31100 | 0.592 | similar to lipase from Dianthus caryophyllus | -0.26 | 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 | -0.33 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.11 | 0 | 0.24 | 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 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -1.95 | 1.95 | 1.69 | -1.28 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | At2g31100 | 266475_at | similar to lipase from Dianthus caryophyllus | 2 | triacylglycerol degradation | Gluconeogenesis from lipids in seeds | Lipid signaling | 0.00 | 3.89 | ||||||||||||||||||||||||||||
At1g59700 | 0.589 | ATGSTU16 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | -3.06 | 0.02 | -0.43 | 0.27 | -0.47 | -0.85 | -0.32 | -0.61 | -0.05 | -0.22 | 0.23 | -0.15 | 1.46 | 0.14 | -0.3 | 0.54 | -0.27 | -0.71 | -0.1 | 0.2 | -0.99 | -0.25 | 0.37 | -0.05 | 0.07 | 0.11 | -0.43 | 0.25 | -0.2 | -0.03 | 0.18 | 0.11 | -0.59 | -0.24 | -0.76 | -0.19 | -0.2 | 0.02 | 0.06 | -0.06 | -0.51 | -0.65 | -0.57 | 0.19 | 0.33 | 0.09 | -1.11 | -0.22 | 0.13 | 0.43 | -0.97 | 0.06 | 0.25 | -0.17 | -0.04 | -0.88 | -0.56 | -0.19 | -0.28 | -0.57 | -0.19 | -0.14 | 0.12 | -0.31 | -0.38 | 0.07 | 0.14 | 0.07 | 0.33 | 0.22 | -0.53 | -0.09 | 0.01 | -0.02 | 0.76 | -0.11 | 0.31 | 0.3 | -0.28 | -0.27 | -0.13 | -0.05 | -0.28 | -0.1 | -0.25 | 0.32 | -0.1 | 0 | 0.52 | 1.01 | -0.2 | -0.04 | -0.15 | 0.32 | -0.31 | 0.02 | 0.13 | 0.38 | -0.28 | 0.05 | 0.63 | -0.01 | -0.24 | -0.03 | 1.12 | 1.65 | 0.94 | 1.06 | -0.54 | 0.55 | 1.06 | 1.53 | 2.21 | 1.74 | 0.04 | 0.01 | 1.12 | 1.59 | 0.92 | 0.84 | -0.87 | 0.1 | 0.52 | 0.48 | 2 | 1.41 | 0.38 | -0.24 | 0.15 | 0.08 | 0.28 | 0.56 | 0.23 | -0.1 | -0.08 | -0.47 | 0.21 | 0.13 | 0.74 | 0.37 | -0.3 | -0.36 | 0.85 | -0.82 | 0.42 | -0.03 | -0.32 | -0.34 | -0.16 | -1.36 | 0.52 | -0.45 | 0.48 | -0.26 | -0.28 | 0.13 | 0.25 | -1.41 | -0.28 | -0.24 | 0.04 | -0.05 | -0.61 | -0.22 | -0.51 | -0.14 | 0.07 | -0.05 | -0.09 | -0.05 | 0.25 | -0.13 | 0.74 | -0.04 | 1.22 | 0.44 | -0.07 | -0.2 | -0.18 | -0.41 | -0.63 | -0.87 | -0.91 | -1.02 | 0.04 | 0.22 | 0.57 | -0.06 | -0.45 | 0.5 | 0.91 | 0.24 | 0.64 | -0.09 | -0.81 | 0.16 | -0.56 | -0.21 | 0.08 | 0.53 | -0.21 | 0.18 | 1.12 | -0.36 | -4.45 | 1.34 | -0.9 | 0.7 | 0.39 | 0.5 | -0.01 | -0.8 | -0.3 | -2.49 | 0.78 | At1g59700 | 262916_at | ATGSTU16 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | 2 | toxin catabolism | Glutathione S-transferase, Tau family | 2.01 | 6.66 | |||||||||||||||||||||||||||
At3g58730 | 0.583 | vacuolar ATP synthase subunit D (VATD) / V-ATPase D subunit / vacuolar proton pump D subunit (VATPD) | -0.63 | -0.07 | 0.13 | -0.1 | 0 | -0.22 | -0.14 | -0.12 | 0.01 | 0.04 | -0.01 | -0.06 | 0.27 | -0.07 | -0.02 | 0.31 | -0.07 | 0 | 0.18 | -0.07 | -0.11 | 0.12 | -0.08 | 0.01 | 0.17 | 0.13 | -0.21 | -0.14 | -0.03 | -0.02 | 0.15 | -0.14 | -0.04 | 0.05 | 0.07 | 0 | 0.05 | 0.06 | 0.05 | -0.09 | 0 | 0.14 | 0.24 | 0.16 | 0.27 | 0.07 | 0.24 | -0.13 | 0.2 | 0.19 | -0.15 | -0.11 | 0.03 | -0.02 | -0.02 | -0.36 | -0.16 | -0.24 | -0.12 | -0.19 | -0.13 | -0.09 | 0.16 | 0.03 | 0.08 | 0.2 | 0.33 | -0.19 | -0.02 | -0.23 | 0.04 | -0.16 | -0.18 | -0.03 | -0.02 | -0.12 | 0.01 | 0.14 | 0.14 | 0.02 | 0.1 | -0.01 | 0 | 0.18 | 0 | -0.16 | -0.09 | -0.1 | 0.09 | -0.1 | -0.04 | 0.04 | 0.02 | -0.18 | 0.15 | 0.02 | -0.24 | -0.26 | -0.04 | -0.08 | 0.03 | 0.08 | 0.2 | -0.02 | 0.14 | 0.3 | 0.53 | 0.69 | -0.09 | -0.12 | 0.01 | -0.25 | 0.01 | -0.02 | 0.06 | -0.04 | 0.01 | 0.34 | 0.5 | 0.57 | -0.15 | -0.27 | -0.12 | -0.34 | 0.06 | 0.07 | 0 | -0.04 | 0.14 | 0.14 | 0.35 | 0.19 | 0.16 | -0.08 | -0.2 | 0.03 | -0.1 | 0.25 | -0.04 | 0.07 | 0.08 | 0.2 | 0.51 | 0.08 | -0.08 | 0.05 | -0.15 | -0.25 | -0.35 | -0.21 | 0.06 | 0.04 | -0.12 | 0 | -0.1 | -0.14 | -0.04 | 0.41 | -0.05 | 0.17 | -0.03 | 0.12 | 0.33 | 0.2 | -0.23 | -0.23 | -0.23 | -0.19 | -0.1 | -0.34 | -0.11 | 0.02 | -0.28 | -0.27 | -0.31 | 0.03 | 0.22 | 0.01 | 0.1 | 0.53 | 0.3 | 0.09 | -0.3 | -0.22 | -0.16 | -0.32 | -0.31 | 0.07 | 0.04 | 0.03 | 0.11 | -0.13 | -0.06 | -0.24 | -0.5 | -0.31 | 0.07 | -0.03 | -0.06 | 0.1 | 0.05 | -0.09 | 0.38 | -0.03 | -1.99 | 1.42 | 0.18 | 0.28 | 0.13 | -0.27 | 0.4 | -0.1 | -0.09 | 0.28 | 0.21 | At3g58730 | 251557_at | vacuolar ATP synthase subunit D (VATD) / V-ATPase D subunit / vacuolar proton pump D subunit (VATPD) | 6 | transport facilitation | transport ATPases | vacuole or lysosome | ATP synthesis | 0.64 | 3.41 | |||||||||||||||||||||||||||||
At4g15490 | 0.579 | UDP-glucoronosyl/UDP-glucosyl transferase family protein, simalr to UDP-glucose:sinapate glucosyltransferase (Brassica napus);Glucosyltransferases for benzoic acids: carboxy-glucosyltransferase 84A3 | -3.53 | 0.15 | -0.08 | -2.14 | -0.64 | -0.96 | -1.08 | -0.95 | -0.39 | -0.4 | 0.15 | -0.51 | 0.76 | -0.6 | -0.14 | -0.34 | -0.53 | -1.4 | 0.11 | 0.1 | -1.42 | -0.37 | 0.01 | 0.21 | 0.14 | 0.47 | -0.42 | 0.15 | 0.22 | 0.13 | 0.35 | 0.31 | 0.27 | -0.03 | -0.34 | -0.24 | -0.24 | -0.05 | 0.03 | -0.1 | -0.38 | -0.69 | -0.38 | 0.53 | 1.3 | 0.01 | -2.12 | 0.41 | 0.49 | 0.42 | -0.64 | 0.05 | 0.23 | -0.38 | 0.16 | -0.68 | -0.65 | -0.38 | -0.51 | -0.56 | -0.32 | 0.31 | 0.32 | -0.14 | -0.28 | 0.61 | 0.57 | 0.08 | 0.24 | -0.24 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | 1.55 | -0.55 | 0.05 | 0.2 | 0.19 | 0.19 | 1.03 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | -0.28 | -0.12 | 0.56 | -0.14 | 0.15 | 0.02 | 0.06 | -0.08 | -0.08 | -0.08 | -0.42 | -0.08 | -0.08 | 0.05 | 0.3 | 1.53 | 1.93 | 1.71 | 2.8 | -0.08 | -0.08 | -0.08 | -0.24 | 0.15 | 0.04 | 0.06 | 0.18 | 1.14 | 0.99 | 1.42 | 2.19 | -0.08 | -0.08 | -0.78 | -0.21 | -0.05 | -0.31 | 0.02 | -0.06 | 1.19 | 0.24 | 1.02 | 0.18 | 0.4 | 0.41 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | -0.26 | -0.08 | 0.3 | -0.05 | 0.99 | 2.1 | -0.37 | -0.87 | 0.01 | 0.82 | 1.3 | 2.64 | -0.08 | -0.08 | -0.08 | -0.3 | -0.08 | -0.08 | -1.39 | -1.03 | -0.08 | -0.32 | -0.07 | -0.88 | 0.12 | -0.66 | -0.22 | -0.09 | 0.13 | -0.08 | -0.08 | -0.28 | 0.28 | -0.08 | -0.08 | -0.08 | -0.08 | 0.23 | -0.1 | -0.15 | 0.36 | 0.1 | 0.3 | 0.69 | 0.77 | -0.08 | -0.08 | -0.08 | -0.08 | -0.08 | -0.28 | -0.08 | 0.08 | 1.09 | 0.57 | -0.16 | 0.84 | -0.56 | -0.97 | 0.17 | -0.71 | -1.11 | 0.18 | -0.07 | -0.32 | -2.36 | -0.39 | 1.15 | 1.29 | 0.65 | -1.2 | -0.15 | 0.35 | -0.25 | -0.76 | -0.43 | At4g15490 | 245352_at | UDP-glucoronosyl/UDP-glucosyl transferase family protein, simalr to UDP-glucose:sinapate glucosyltransferase (Brassica napus);Glucosyltransferases for benzoic acids: carboxy-glucosyltransferase 84A3 | 10 | C-compound and carbohydrate utilization | Phenylpropanoid Metabolism | Glucosyltransferases for benzoic acids | Glycosyl transferase, Family 1 | 2.28 | 6.33 | ||||||||||||||||||||||||||||
At1g66670 | 0.569 | CLPP3 | One of several nuclear-encoded ClpPs (caseinolytic protease). Contains a highly conserved catalytic triad of Ser-type proteases (Ser-His-Asp). The name reflects nomenclature described in Adam et. al (2001). | -1.29 | 0.13 | 0.18 | 0.98 | 0.07 | -0.38 | -0.26 | -0.16 | -0.56 | -0.34 | -0.28 | -0.16 | -0.2 | -0.17 | -0.42 | -0.11 | -0.01 | 0.16 | 0.41 | -0.24 | -0.27 | 0.53 | 0.02 | -0.15 | 0 | 0.49 | 0.14 | -0.06 | -0.07 | -0.04 | 0.36 | 0.11 | 0.4 | 0.12 | 0 | 0.08 | 0.06 | 0.19 | 0.24 | 0.05 | -0.07 | 0.25 | 0.21 | 0.22 | 0.26 | 0.07 | -0.1 | -0.04 | 0.47 | 0.26 | -0.17 | 0.1 | 0.03 | -0.02 | -0.05 | -0.09 | -0.45 | 0 | -0.36 | -0.04 | -0.3 | 0.18 | 0.01 | 0.27 | 0.21 | -0.06 | 0.11 | -0.05 | 0.24 | -0.05 | -0.03 | 0.08 | 0.22 | 0.04 | 0.05 | -0.11 | 0.01 | -0.05 | 0.13 | 0.14 | -0.03 | -0.17 | -0.12 | -0.37 | 0.06 | 0.13 | -0.1 | -0.19 | 0.04 | -0.27 | -0.43 | -0.21 | -0.1 | -0.08 | -0.09 | -0.09 | -0.1 | 0.01 | 0.02 | -0.01 | 0.02 | -0.37 | 0.09 | 0.26 | -0.07 | -0.16 | -0.23 | -0.12 | -0.02 | -0.03 | -0.06 | 0.13 | 0.08 | 0.01 | -0.13 | -0.03 | 0 | -0.27 | -0.15 | -0.42 | -0.12 | -0.17 | -0.51 | -0.42 | -0.06 | -0.47 | -0.07 | 0.35 | -0.19 | -0.17 | 0.12 | -0.11 | -0.07 | -0.35 | -0.03 | -0.26 | -0.09 | -0.02 | 0.16 | -0.08 | -0.16 | 0.04 | -0.67 | 0.23 | 0.27 | 0.4 | 0.04 | -0.18 | -0.66 | -0.43 | 0.06 | 0.11 | 0.17 | -0.17 | 0.19 | 0.3 | 0.37 | 0.14 | 0.38 | 0.21 | 0.74 | 0.24 | 0.15 | -0.1 | 0.33 | 0.1 | 0.19 | 0.13 | -0.09 | 0.1 | -0.28 | -0.55 | 0.22 | 0.15 | 0.4 | 0.28 | 0.09 | -0.05 | -0.14 | -0.16 | 0 | 0.42 | -0.11 | 0.01 | -0.2 | -0.19 | 0.02 | -0.14 | -0.2 | -0.16 | -0.14 | 0.53 | 0 | -0.12 | -0.23 | -0.48 | 0.18 | 0.26 | 0.18 | -0.4 | 0.31 | 0.16 | 0.44 | -0.28 | -4.01 | 2.93 | 1.17 | 1.31 | 0.14 | -0.01 | 0.42 | 0.02 | -0.08 | 0.54 | 0.43 | At1g66670 | 256411_at | CLPP3 | One of several nuclear-encoded ClpPs (caseinolytic protease). Contains a highly conserved catalytic triad of Ser-type proteases (Ser-His-Asp). The name reflects nomenclature described in Adam et. al (2001). | 4 | chloroplastic endopeptidase Clp complex | ATP-dependent proteolysis | Chloroplastic protein turnover | ClpP protease complex | 0.86 | 6.95 | |||||||||||||||||||||||||||
At1g78670 | 0.566 | similar to gamma glutamyl hydrolase from Glycine max | -1.21 | 0.27 | 0.15 | -0.11 | -0.48 | -0.87 | -0.82 | -0.87 | -0.74 | -0.6 | 0.05 | -0.37 | 0.77 | 0.07 | -0.28 | 0.23 | -0.41 | -0.45 | -0.19 | -0.12 | -0.82 | -0.34 | 0.22 | -0.4 | -0.55 | 0.12 | -0.03 | 0.15 | -0.2 | -0.41 | -0.05 | 0.16 | -0.09 | 0.38 | -0.18 | -0.18 | -0.3 | -0.28 | -0.03 | -0.16 | -0.56 | -0.75 | -0.84 | 0.41 | 0.99 | 0 | -0.84 | 0.21 | 0.64 | 0.59 | -0.28 | 0.13 | 0.27 | -0.06 | 0.05 | -0.32 | -0.69 | -0.32 | -0.74 | -0.36 | -0.57 | 0.15 | -0.02 | 0.02 | -0.42 | 0.26 | 0.57 | 0.41 | 0.43 | 0.73 | 0.35 | 0.13 | 0.28 | 0.36 | 0.32 | 0.66 | 0.33 | 0.13 | -0.13 | -0.15 | -0.18 | -0.01 | -0.02 | -0.13 | -0.09 | 0.19 | 0.26 | 0.06 | 0.25 | 0.22 | -0.27 | -0.06 | -0.43 | 0.02 | 0.39 | 0.35 | 0.02 | 0.13 | 0.01 | -0.06 | 0.25 | 0.32 | -0.18 | -0.28 | 0.87 | 1.64 | 1.38 | 1.92 | -0.48 | -0.42 | -0.11 | 0.13 | 0.45 | 0.45 | 0.09 | 0.15 | 1.03 | 1.21 | 0.9 | 1.41 | -0.2 | -0.25 | -0.88 | -1.44 | -0.03 | -0.22 | 0.54 | -0.3 | -0.32 | -0.26 | 0.5 | 0.75 | 0.43 | 0.41 | 0 | -0.34 | -0.31 | -0.07 | 0.07 | 0.23 | 0.07 | -0.07 | 1.54 | -0.04 | -0.38 | -0.04 | -0.2 | -0.91 | -1.12 | -1.49 | -1.28 | 0.09 | 0 | -0.41 | -0.27 | -0.35 | -0.68 | -0.44 | -0.27 | -0.56 | 0.28 | 0.01 | 0.17 | -0.28 | 1 | 0.36 | 0.47 | 0.09 | 0.43 | 0.13 | 0.12 | -0.13 | 0.44 | 0.39 | 0.81 | 0.46 | -0.25 | -0.5 | -0.49 | -0.28 | -0.11 | -0.1 | 0.17 | -0.09 | 0.16 | 0.02 | 0.05 | -0.23 | 0.37 | 0.52 | 0.38 | 0.12 | 0.39 | -0.13 | -0.92 | -0.44 | -0.22 | -0.36 | 0.66 | 0.43 | 0.12 | -0.05 | 0.5 | -0.42 | -1.72 | 1.21 | -0.31 | 1.23 | 0.41 | 0.56 | -0.03 | -0.14 | 0.06 | -0.77 | 0.1 | At1g78670 | 264300_at | similar to gamma glutamyl hydrolase from Glycine max | 4 | Folate biosynthesis | 1.77 | 3.64 | ||||||||||||||||||||||||||||||
At2g24820 | 0.566 | similar to Rieske iron-sulfur protein Tic55 from Pisum sativum | -1.87 | 0.11 | 0.05 | 0 | -0.18 | -0.8 | -0.64 | -0.6 | -0.83 | -0.48 | -0.32 | -0.22 | 0.27 | -0.45 | -0.95 | -0.13 | -0.4 | -0.46 | -0.41 | -0.33 | -1.08 | -0.48 | -0.04 | -0.33 | -0.32 | 0.06 | -0.12 | 0.1 | -0.15 | -0.37 | -0.48 | -0.1 | -0.01 | -0.2 | -0.45 | 0.09 | 0.09 | 0.28 | 0.15 | 0.03 | -0.22 | -0.09 | -0.22 | 0.01 | -0.26 | -0.1 | -0.55 | -0.62 | 0 | 0.01 | -0.11 | 0.23 | 0.12 | -0.06 | -0.12 | -0.43 | -0.9 | -0.13 | -0.81 | -0.38 | -0.59 | 0.32 | 0 | 0.22 | -0.16 | -0.28 | -0.11 | 0.03 | 0.24 | 0.25 | 0.2 | 0.33 | 0.23 | 0.08 | 0.22 | 0.1 | 0.3 | -0.77 | 0.04 | -0.01 | 0.24 | 0.23 | 0.02 | 0.02 | 0.23 | 0.13 | 0.11 | 0.09 | -0.09 | 0.33 | -0.15 | -0.19 | 0.38 | 0.38 | 0.22 | 0.2 | 0.02 | 0.11 | 0.21 | 0.15 | 0.1 | 0.35 | 0.13 | -0.03 | 0.38 | 0.81 | 0.16 | 0.26 | 0.26 | 0.05 | 0.49 | 0.75 | 0.73 | 1.06 | 0.05 | 0.05 | 0.37 | 0.38 | 0.06 | 0.17 | 0.31 | 0.23 | 0.05 | -0.37 | 0.64 | 1.04 | 0.12 | 0.53 | 0.15 | 0.13 | 0.47 | 0.33 | 0.26 | 0.01 | 0.17 | -0.17 | -0.07 | 0.03 | 0.33 | 0.14 | -0.04 | -0.6 | -0.53 | 0.28 | 0.08 | 0.34 | -0.07 | -0.09 | -0.16 | -0.67 | -0.62 | 0.27 | 0.44 | 0.53 | 0.2 | -0.1 | 0.16 | -1.27 | 0.07 | -0.21 | 0.75 | 0.32 | -0.28 | -0.6 | -0.06 | 0.08 | 0.03 | 0.15 | 0.47 | 0.44 | -0.01 | 0.01 | 0.56 | 0.49 | 0.38 | 0.42 | 0.19 | -0.02 | 0.15 | 0.02 | 0.5 | 0.52 | 0.1 | 0.31 | 0.17 | 0.49 | 0.66 | 0.15 | -0.06 | -0.01 | 0.21 | 0.51 | 0.24 | -0.26 | -0.32 | -0.5 | -0.12 | 0.02 | -0.16 | -0.02 | -0.53 | 0.19 | 0.08 | -0.84 | -2.5 | 1.14 | 0 | 1.49 | 0.11 | -0.07 | 0.37 | -0.2 | -0.1 | -1.04 | 0.35 | At2g24820 | 263533_at (m) | similar to Rieske iron-sulfur protein Tic55 from Pisum sativum | 4 | Chloroplastic protein import via envelope membrane | Tic apparatus | 1.31 | 3.99 | ||||||||||||||||||||||||||||||
At3g55290 | 0.566 | short-chain dehydrogenase/reductase (SDR) family protein, contains similarity to 3-oxoacyl-(acyl-carrier protein) reductase (Bacillus subtilis) | -1.4 | NA | -0.06 | -0.88 | -0.12 | -0.23 | -0.33 | -0.24 | 0.17 | -0.66 | 0.14 | 0.12 | 3.1 | -0.1 | 0.6 | 1.42 | -0.12 | -0.61 | 0.21 | -0.12 | -0.83 | -0.12 | 0.01 | -0.03 | 0.13 | -0.04 | -0.24 | 0.41 | -0.13 | 0.13 | -0.12 | -0.24 | -0.12 | -0.12 | -0.12 | -0.04 | -0.02 | 0.14 | -0.12 | -0.12 | -0.3 | -0.21 | -0.93 | 0.25 | 1.1 | 1.25 | 0.17 | -0.12 | -0.36 | -0.12 | -0.39 | 0.35 | -0.04 | -0.12 | -0.5 | -0.12 | -0.85 | 0.14 | -0.73 | -0.12 | -0.41 | -0.12 | -0.53 | -0.62 | -0.28 | 0.17 | 0.65 | 0.41 | -0.14 | 0.31 | -0.07 | 0.13 | -0.63 | 0.43 | 0.48 | 1.37 | 0.32 | 0.6 | -0.18 | -0.34 | -0.18 | 0.13 | -0.61 | -0.05 | -0.12 | -1.09 | -0.21 | -0.25 | 0.21 | 0.28 | -0.34 | -0.16 | -0.48 | 0.25 | -0.09 | -0.12 | 0.71 | 0.07 | 0.73 | 0.05 | 0.53 | -0.18 | -1.07 | -0.27 | 0.48 | 1.99 | 2.27 | 2.79 | -0.37 | -1.25 | -0.01 | -0.54 | 0.8 | 0.9 | 0.01 | 0.11 | 1.36 | 2.22 | 1.38 | 1.71 | 0.23 | -1.02 | -0.56 | -1.52 | 0.49 | 0.21 | 0.28 | -0.7 | 0.04 | 0.37 | 1.88 | 1.52 | 0.69 | 0.64 | -0.21 | -0.28 | -0.83 | 0.51 | 0.67 | 1.33 | 0.49 | 0.09 | -0.1 | 0.68 | 0.72 | 0.04 | -0.03 | -0.84 | -0.36 | -0.23 | 0.81 | 0.54 | -0.1 | 0.47 | 0.21 | 0.3 | -0.33 | -0.36 | 0.56 | -0.12 | -0.74 | -0.46 | -1.13 | -0.93 | -0.5 | 0.09 | 0.78 | -0.19 | 0.4 | -0.56 | -0.8 | -0.65 | -0.9 | -1.02 | -0.16 | -0.26 | -0.71 | -0.82 | -1.02 | -1.5 | -0.89 | -1.29 | -0.37 | -0.64 | 0.13 | 1.52 | -0.43 | 0.5 | -0.2 | 0.77 | -0.18 | -1.08 | 0.23 | -0.33 | -1.66 | -1.37 | -0.54 | -0.3 | -0.12 | -0.12 | -0.18 | 0.39 | -0.11 | -0.02 | -3.6 | 2.98 | 1.51 | 0.44 | -0.26 | 0.08 | -0.16 | -0.2 | -0.12 | -1.61 | 1.47 | At3g55290 | 251780_s_at (m) | short-chain dehydrogenase/reductase (SDR) family protein, contains similarity to 3-oxoacyl-(acyl-carrier protein) reductase (Bacillus subtilis) | 2 | Leaf Glycerolipid Biosynthesis | Leaf Glycerolipid Biosynthesis in Plastid | Synthesis of fatty acids in plastids | 2.56 | 6.71 | |||||||||||||||||||||||||||||
At3g55310 | 0.566 | short-chain dehydrogenase/reductase (SDR) family protein, contains similarity to 3-oxoacyl-(acyl-carrier protein) reductase (Bacillus subtilis) | -1.4 | NA | -0.06 | -0.88 | -0.12 | -0.23 | -0.33 | -0.24 | 0.17 | -0.66 | 0.14 | 0.12 | 3.1 | -0.1 | 0.6 | 1.42 | -0.12 | -0.61 | 0.21 | -0.12 | -0.83 | -0.12 | 0.01 | -0.03 | 0.13 | -0.04 | -0.24 | 0.41 | -0.13 | 0.13 | -0.12 | -0.24 | -0.12 | -0.12 | -0.12 | -0.04 | -0.02 | 0.14 | -0.12 | -0.12 | -0.3 | -0.21 | -0.93 | 0.25 | 1.1 | 1.25 | 0.17 | -0.12 | -0.36 | -0.12 | -0.39 | 0.35 | -0.04 | -0.12 | -0.5 | -0.12 | -0.85 | 0.14 | -0.73 | -0.12 | -0.41 | -0.12 | -0.53 | -0.62 | -0.28 | 0.17 | 0.65 | 0.41 | -0.14 | 0.31 | -0.07 | 0.13 | -0.63 | 0.43 | 0.48 | 1.37 | 0.32 | 0.6 | -0.18 | -0.34 | -0.18 | 0.13 | -0.61 | -0.05 | -0.12 | -1.09 | -0.21 | -0.25 | 0.21 | 0.28 | -0.34 | -0.16 | -0.48 | 0.25 | -0.09 | -0.12 | 0.71 | 0.07 | 0.73 | 0.05 | 0.53 | -0.18 | -1.07 | -0.27 | 0.48 | 1.99 | 2.27 | 2.79 | -0.37 | -1.25 | -0.01 | -0.54 | 0.8 | 0.9 | 0.01 | 0.11 | 1.36 | 2.22 | 1.38 | 1.71 | 0.23 | -1.02 | -0.56 | -1.52 | 0.49 | 0.21 | 0.28 | -0.7 | 0.04 | 0.37 | 1.88 | 1.52 | 0.69 | 0.64 | -0.21 | -0.28 | -0.83 | 0.51 | 0.67 | 1.33 | 0.49 | 0.09 | -0.1 | 0.68 | 0.72 | 0.04 | -0.03 | -0.84 | -0.36 | -0.23 | 0.81 | 0.54 | -0.1 | 0.47 | 0.21 | 0.3 | -0.33 | -0.36 | 0.56 | -0.12 | -0.74 | -0.46 | -1.13 | -0.93 | -0.5 | 0.09 | 0.78 | -0.19 | 0.4 | -0.56 | -0.8 | -0.65 | -0.9 | -1.02 | -0.16 | -0.26 | -0.71 | -0.82 | -1.02 | -1.5 | -0.89 | -1.29 | -0.37 | -0.64 | 0.13 | 1.52 | -0.43 | 0.5 | -0.2 | 0.77 | -0.18 | -1.08 | 0.23 | -0.33 | -1.66 | -1.37 | -0.54 | -0.3 | -0.12 | -0.12 | -0.18 | 0.39 | -0.11 | -0.02 | -3.6 | 2.98 | 1.51 | 0.44 | -0.26 | 0.08 | -0.16 | -0.2 | -0.12 | -1.61 | 1.47 | At3g55310 | 251780_s_at (m) | short-chain dehydrogenase/reductase (SDR) family protein, contains similarity to 3-oxoacyl-(acyl-carrier protein) reductase (Bacillus subtilis) | 2 | lipid, fatty acid and isoprenoid biosynthesis | fatty acid biosynthesis | Leaf Glycerolipid Biosynthesis | Leaf Glycerolipid Biosynthesis in Plastid | Synthesis of fatty acids in plastids | 2.56 | 6.71 | ||||||||||||||||||||||||||||
At4g29010 | 0.563 | AIM1 | Functions in beta-oxidation of fatty acids, similar to CuMFP with L-3-hydroxyacyl-CoA hydrolyase , L-3-hydroxyacyl-dehydrogenase, D-3-hydroxyacyl-CoA epimerase, and 3, 2-enoyl-CoA isomerase activities; abnormal inflorescence meristem 1 / fatty acid multifunctional protein (AIM1) | -1.02 | 0.03 | 0.25 | -0.18 | 0.18 | -0.4 | -0.36 | -0.11 | -0.1 | -0.11 | 0.27 | -0.25 | 0.37 | -0.09 | -0.28 | 0.47 | 0.11 | -0.06 | 0.08 | 0.1 | -0.21 | 0.14 | -0.1 | -0.08 | 0.03 | 0.14 | 0 | -0.02 | 0.07 | -0.12 | 0.21 | 0.06 | -0.14 | 0.13 | -0.01 | -0.15 | 0.01 | 0.09 | 0.15 | 0.05 | -0.13 | -0.44 | -0.22 | 0.2 | 0.54 | 0.12 | -0.53 | 0.32 | 0.46 | 0.6 | -0.1 | 0.05 | 0.28 | 0.1 | 0.41 | -0.16 | 0.28 | -0.24 | 0.31 | -0.02 | 0.6 | 0.32 | 0.36 | -0.16 | -0.71 | -0.16 | 0.22 | -0.3 | 0.27 | -0.07 | 0.09 | -0.04 | -0.09 | -0.01 | 0.01 | -0.14 | 0.05 | 0.1 | -0.2 | 0.06 | 0.28 | -0.12 | 0.23 | 0.02 | 0.06 | 0.12 | 0.06 | 0.03 | 0.04 | 0.08 | -0.11 | 0.38 | 0.22 | 0.02 | 0.34 | 0.26 | -0.09 | 0.03 | 0 | 0.12 | 0.09 | 0.28 | -0.22 | 0.04 | 0.17 | 0.56 | 1.2 | 1.54 | -0.22 | -0.05 | 0.27 | 0.56 | 0.52 | 0.74 | -0.05 | -0.05 | 0.54 | 0.41 | 0.74 | 0.79 | -0.23 | -0.07 | -0.21 | -0.4 | 0.32 | 0.42 | -0.32 | -0.2 | -0.16 | 0.04 | 0.41 | 0.28 | 0.4 | 0.4 | 0.03 | -0.09 | -0.07 | 0.01 | 0.2 | 0.08 | 0.1 | -0.26 | 0.95 | -0.23 | -0.77 | -0.08 | -0.3 | -0.68 | -1.11 | -0.05 | -0.73 | -0.13 | -0.1 | -0.24 | -0.27 | -0.32 | -0.26 | -0.09 | 0.32 | 0.24 | 0.27 | 0.04 | 0.13 | -0.59 | -0.27 | -0.26 | 0.18 | -0.3 | 0.17 | -0.01 | -0.33 | -0.91 | -0.44 | 0.28 | 0.23 | 0.22 | -0.28 | -0.56 | -0.87 | -1.4 | -1 | -0.42 | -0.01 | 0.12 | -0.1 | -0.2 | -0.11 | -0.15 | 0.17 | 0.12 | 0.12 | -0.06 | -0.14 | -0.13 | -0.91 | -0.69 | 0.28 | -0.09 | 0.12 | 0.17 | -0.26 | 0.17 | 0.56 | 0.24 | -2.15 | 0.55 | 0.21 | 0.55 | 0.15 | -0.05 | -0.05 | -0.14 | 0.46 | -0.1 | -0.48 | At4g29010 | 253759_at | AIM1 | Functions in beta-oxidation of fatty acids, similar to CuMFP with L-3-hydroxyacyl-CoA hydrolyase , L-3-hydroxyacyl-dehydrogenase, D-3-hydroxyacyl-CoA epimerase, and 3, 2-enoyl-CoA isomerase activities; abnormal inflorescence meristem 1 / fatty acid multifunctional protein (AIM1) | 9 | enoyl-CoA hydratase activity | flower development | seed germination | oxidation of fatty acids | isoleucine degradation III | isoleucine degradation I | valine degradation II | valine degradation I | fatty acid oxidation pathway | Gluconeogenesis from lipids in seeds | fatty acid beta oxidation complex | Degradation of storage lipids and straight fatty acids | 1.25 | 3.69 | ||||||||||||||||||||||||
At1g67280 | 0.555 | similar to putative lactoylglutathione lyase from Brassica oleracea | -1.25 | 0.06 | 0.1 | 0.7 | -0.15 | -0.44 | -0.34 | -0.21 | -0.7 | -0.55 | -0.19 | -0.07 | -0.59 | -0.25 | -0.45 | -0.72 | -0.11 | -0.22 | -0.3 | -0.22 | -0.46 | -0.35 | -0.05 | -0.19 | -0.3 | -0.04 | 0 | -0.14 | -0.15 | -0.17 | -0.02 | -0.01 | -0.19 | 0.11 | -0.05 | 0.12 | 0.14 | 0.12 | 0.12 | 0.16 | -0.12 | -0.14 | -0.22 | -0.15 | -0.47 | -0.07 | -0.62 | -0.44 | -0.25 | -0.11 | -0.26 | 0.22 | 0.01 | -0.13 | -0.11 | -0.07 | -0.63 | -0.03 | -0.72 | -0.04 | -0.62 | 0.16 | -0.12 | 0.02 | -0.21 | -0.1 | -0.48 | -0.39 | -0.09 | -0.22 | 0.61 | -0.02 | -0.08 | 0.06 | 0.4 | 0.49 | 0.22 | -0.18 | 0.04 | 0.22 | 0.41 | 0.34 | 0.34 | 0.11 | 0.1 | 0.07 | 0.21 | 0.22 | 0.25 | 0.28 | 0.31 | 0.44 | 0.16 | 0.41 | 0.25 | -0.11 | -0.04 | 0.16 | -0.04 | 0.07 | 0.14 | -0.08 | 0 | 0.17 | 0.06 | 0.17 | 0.01 | 0.44 | -0.26 | -0.01 | 0.2 | 0.35 | 0.5 | 0.36 | 0.09 | 0.36 | 0.28 | 0.22 | -0.03 | -0.06 | 0.01 | 0 | 0.1 | -0.28 | 0.43 | 0.11 | -0.12 | 0.13 | 0.26 | 0.42 | 0.43 | 0.37 | 0.07 | -0.04 | 0.33 | 0 | 0.22 | 0.46 | 0.08 | 0.05 | 0.01 | -0.24 | -0.04 | -0.03 | -0.28 | 0.41 | 0.2 | -0.27 | -0.11 | -0.52 | -0.27 | -0.14 | 0.07 | 0 | -0.14 | -0.1 | -0.17 | -0.54 | -0.12 | -0.13 | 0.24 | 0.37 | 0.49 | -0.04 | -0.23 | -0.11 | 0.37 | 0.11 | 0.45 | -0.1 | 0.24 | 0.24 | 0.34 | 0.21 | 0.53 | 0.16 | 0.15 | 0.1 | 0.04 | 0.54 | 0.18 | 0.16 | 0.15 | 0.27 | 0.15 | -0.02 | 0.25 | 0.16 | 0.39 | 0.25 | 0.21 | 0.08 | 0.07 | 0.12 | -0.32 | -0.31 | -0.14 | -0.26 | 0.05 | 0.1 | 0.14 | 0 | -0.05 | -0.59 | -3.7 | 2.25 | 0.59 | 0.61 | 0.3 | -0.17 | -0.04 | -0.59 | 0.21 | -0.14 | 0.02 | At1g67280 | 264970_at | similar to putative lactoylglutathione lyase from Brassica oleracea | 4 | vitamin E biosynthesis | plastoquinone biosynthesis | phenylalanine degradation I | threonine degradation | tyrosine degradation | methylglyoxal degradation | methylglyoxal pathway | 1.01 | 5.95 | ||||||||||||||||||||||||||||||
At1g20560 | 0.548 | AMP-dependent synthetase and ligase family protein | 0.06 | 0.22 | 0.17 | -0.11 | -0.54 | -1.43 | -0.77 | -0.94 | -0.62 | -0.4 | 0.01 | -0.54 | 1.09 | 0.56 | 0.38 | 0.09 | -0.45 | -0.47 | -0.35 | -0.35 | -0.86 | -0.67 | 0.3 | -0.38 | -0.14 | 0.1 | -0.39 | 0.46 | 0.03 | -0.12 | 0.05 | 0.32 | -0.08 | -0.02 | -0.31 | -0.01 | 0.04 | 0.02 | 0.12 | 0.27 | -0.24 | -0.38 | -0.56 | 0.46 | 0.6 | -0.06 | -0.6 | 0.26 | 0.74 | 0.22 | -0.22 | 0.27 | 0.04 | -0.21 | 0.01 | -0.24 | -0.52 | -0.02 | -0.48 | -0.18 | -0.48 | 0.34 | -0.04 | 0.23 | -0.39 | -0.19 | 0.41 | 0.54 | 0.6 | 0.62 | 0.44 | 0.21 | 0.18 | 0.27 | 0.16 | -0.02 | 0.1 | 0.83 | -0.14 | 0.04 | -0.02 | 0.05 | -0.01 | -0.03 | 0.25 | 0.28 | 0.11 | 0.06 | -0.07 | 0.09 | -0.08 | 0.14 | 0.06 | 0.04 | 0.08 | 0.02 | 0.11 | 0.23 | 0.18 | -0.25 | -0.19 | -0.04 | -0.28 | -0.55 | 0.3 | 0.84 | 1.32 | 1.4 | -0.04 | -0.07 | -0.54 | -0.44 | -0.42 | 0.06 | -0.14 | -0.11 | 0.43 | 0.75 | 0.97 | 0.8 | 0.07 | 0.25 | -0.05 | -0.71 | -0.56 | -0.21 | 0.02 | 0.43 | -0.26 | -0.28 | 0.26 | 0.28 | 0.43 | 0.16 | 0.36 | 0.02 | -0.02 | 0.02 | 0.04 | 0 | 0.12 | -0.25 | 1.33 | -0.05 | -1 | 0 | -0.02 | -0.36 | -0.69 | -1.62 | -2.16 | 0.35 | 0.28 | 0.28 | -0.28 | -0.97 | -1.58 | -0.54 | 0.01 | -0.16 | 0.5 | -0.11 | -0.42 | -0.54 | -0.08 | 0.23 | 0.04 | -0.25 | 0.38 | 0.21 | 0.35 | 0.42 | 0.35 | 0.37 | 0 | 0.04 | 0.11 | -0.06 | -0.14 | -0.28 | -0.24 | -0.41 | 0.06 | 0.18 | 0.57 | 0.18 | 0.36 | 0.4 | 0.45 | 0.24 | 0.15 | 0.6 | 0.07 | -0.3 | -0.48 | -0.15 | 0.13 | -0.23 | -0.03 | 0.01 | -0.12 | 0.21 | 0.61 | 0.09 | -1.97 | 2.44 | 0.2 | 0.76 | 0.04 | 0.09 | -0.24 | -0.14 | 0.39 | -1.19 | 1 | At1g20560 | 259545_at | AMP-dependent synthetase and ligase family protein | 2 | carnitine metabolism-- CoA-linked | Acyl activating enzymes , CoA ligases, clade VI | 1.48 | 4.60 | |||||||||||||||||||||||||||||
At4g33670 | 0.539 | L-galactose dehydrogenase (L-GalDH) | -0.59 | 0.05 | 0.06 | 0.08 | -0.57 | -0.86 | -0.57 | -0.33 | -0.7 | -0.63 | -0.39 | 0 | -0.47 | -0.26 | -0.59 | -0.41 | -0.28 | -0.01 | -0.32 | -0.36 | -0.7 | -0.35 | 0.02 | -0.11 | -0.26 | -0.2 | 0.01 | -0.03 | 0.04 | -0.28 | -0.35 | -0.16 | -0.14 | 0.28 | -0.25 | 0.23 | 0.35 | 0.23 | 0.31 | 0.18 | 0.15 | -0.01 | -0.07 | -0.11 | -0.22 | 0.1 | -0.33 | -0.15 | 0.2 | -0.01 | -0.05 | 0.23 | -0.12 | 0.13 | -0.28 | -0.01 | -0.81 | 0.04 | -0.84 | 0 | -0.57 | 0.09 | -0.17 | 0.01 | -0.09 | -0.21 | -0.25 | -0.1 | 0.08 | -0.08 | 0.25 | -0.12 | 0.1 | 0.16 | 0.2 | 0.22 | 0.12 | -0.45 | 0.05 | 0.21 | 0.21 | 0.26 | 0.13 | 0.03 | -0.07 | 0.16 | 0.22 | 0.11 | 0.1 | 0.32 | 0.43 | 0.41 | 0.11 | 0.13 | 0.06 | -0.14 | -0.09 | 0.22 | 0.19 | 0.02 | 0.15 | 0.16 | 0.05 | 0.28 | -0.22 | 0.05 | 0.05 | 0.65 | -0.19 | 0.12 | 0.28 | 0.18 | 0.52 | 0.34 | 0.2 | 0.5 | 0.25 | 0.06 | 0.28 | 0.39 | 0.03 | 0.22 | -0.19 | -0.28 | -0.02 | -0.05 | 0.15 | -0.23 | -0.08 | 0.07 | 0.07 | 0.32 | 0.21 | 0.26 | 0.23 | -0.17 | 0.15 | 0.08 | 0.1 | 0.13 | 0.06 | -0.27 | 0.72 | -0.67 | -1.01 | 0.1 | 0.05 | -0.75 | -0.76 | -0.36 | 0.28 | 0.02 | 0.08 | -0.13 | -0.38 | -0.08 | -0.18 | -0.04 | 0.3 | 0.28 | 0.18 | 0.28 | 0.44 | 0.12 | 0.13 | 0.08 | -0.03 | -0.12 | 0.44 | -0.03 | 0.32 | 0.41 | 0.47 | 0.38 | 0.38 | 0.15 | 0.04 | 0.12 | 0.2 | 0.33 | 0.12 | -0.01 | 0.22 | 0.22 | 0.18 | 0.01 | 0.31 | 0.2 | 0.06 | 0.25 | 0.11 | -0.09 | -0.06 | 0.25 | -0.81 | -0.74 | 0.12 | 0.17 | 0.16 | 0.33 | 0.35 | -0.01 | 0.41 | 0.21 | -2.92 | 1.96 | 0.6 | 0.22 | 0.2 | 0.02 | 0.14 | -0.37 | 0.21 | -0.75 | 0.21 | At4g33670 | 253307_at | L-galactose dehydrogenase (L-GalDH) | 8 | Cell Wall Carbohydrate Metabolism | ascorbic acid biosynthesis | 1.11 | 4.88 | ||||||||||||||||||||||||||||||
At5g43940 | 0.536 | ADHIII | alcohol dehydrogenase class III / glutathione-dependent formaldehyde dehydrogenase / GSH-FDH (ADHIII) | 0.22 | 0.03 | 0.16 | 0.14 | -0.21 | -0.28 | -0.21 | -0.23 | -0.17 | -0.01 | -0.05 | -0.08 | -0.28 | -0.06 | 0.02 | -0.26 | -0.09 | 0.02 | 0.1 | -0.13 | -0.42 | -0.14 | -0.05 | 0.17 | 0.11 | 0.08 | -0.07 | 0.01 | 0.1 | 0.14 | 0.31 | 0.13 | 0.28 | 0.12 | -0.22 | 0.04 | 0 | -0.11 | 0.12 | 0.15 | 0.07 | -0.02 | 0.07 | 0.21 | 0.3 | 0.02 | 0.04 | 0.13 | 0.25 | 0.57 | -0.15 | 0.01 | -0.04 | -0.06 | -0.04 | -0.3 | -0.46 | -0.16 | -0.48 | -0.22 | -0.44 | 0.05 | -0.07 | 0.1 | 0.06 | 0 | -0.07 | -0.2 | 0.15 | 0.12 | -0.06 | 0.19 | 0.02 | 0.01 | 0.21 | -0.22 | -0.16 | 0.19 | 0.12 | -0.01 | 0.16 | -0.08 | 0.1 | 0.06 | 0.08 | 0.02 | 0 | 0.01 | -0.06 | 0.05 | 0.14 | 0.12 | 0.02 | 0.01 | 0.25 | 0.24 | 0.11 | 0.08 | -0.05 | 0.07 | 0.05 | 0.19 | 0.08 | 0.1 | 0.23 | 0.18 | 0.2 | 0.49 | 0.03 | -0.11 | -0.14 | 0 | -0.18 | -0.17 | 0.13 | 0.15 | 0.32 | 0.19 | 0.39 | 0.48 | 0 | -0.23 | -0.57 | -0.94 | -0.3 | -0.32 | -0.04 | 0.06 | 0.23 | 0.11 | 0.31 | 0 | 0.24 | 0.15 | -0.18 | 0.05 | -0.13 | -0.1 | 0.19 | 0.02 | 0.15 | -0.1 | 0.46 | -0.11 | -0.02 | 0.28 | 0.1 | -0.39 | -0.66 | -0.63 | -0.46 | 0.04 | -0.19 | -0.07 | -0.2 | -0.23 | -0.3 | -0.24 | 0.16 | 0.35 | 0.39 | 0.25 | -0.04 | -0.3 | 0.02 | -0.33 | 0.09 | 0.18 | 0 | 0.07 | 0.17 | -0.24 | -0.04 | 0.05 | 0.03 | 0.14 | 0 | -0.05 | -0.2 | -0.28 | -0.38 | -0.55 | 0 | -0.27 | -0.22 | 0.09 | -0.02 | -0.2 | 0.23 | 0.12 | -0.06 | 0.2 | 0.15 | -0.07 | -0.23 | -0.09 | 0.44 | 0.25 | 0.11 | -0.05 | -0.21 | 0.25 | 0.77 | 0.23 | -1.83 | 0.96 | 0.41 | 0.56 | 0.03 | -0.13 | 0.21 | 0.01 | -0.08 | -0.67 | 0.55 | At5g43940 | 249077_at | ADHIII | alcohol dehydrogenase class III / glutathione-dependent formaldehyde dehydrogenase / GSH-FDH (ADHIII) | 9 | formaldehyde dehydrogenase (glutathione) activity | C-compound and carbohydrate metabolism | fermentation | Glycolysis / Gluconeogenesis | Pyruvate metabolism | Methane metabolism | Fatty acid metabolism | Bile acid biosynthesis | Glycerolipid metabolism | Tyrosine metabolism | 1- and 2-Methylnaphthalene degradation | 0.81 | 2.80 | ||||||||||||||||||||||||||
At1g64970 | 0.531 | G-TMT | gamma-tocopherol methyltransferase (g-TMT), nuclear; mutant is deficient in alpha and beta tocopherol; Accumulates gamma tocopherol in leaves | -1.77 | 0.1 | 0 | -0.02 | -0.06 | -0.27 | -0.06 | -0.14 | -1.12 | -0.56 | -0.2 | -0.15 | 0.49 | -0.45 | -0.23 | 0.1 | -0.43 | -0.52 | -0.08 | -0.2 | -0.78 | -0.36 | 0.23 | 0.08 | -0.11 | -0.12 | 0.01 | 0.04 | 0.01 | -0.24 | -0.15 | 0.33 | 0.13 | -0.15 | -0.43 | -0.37 | -0.36 | -0.32 | -0.15 | -0.33 | -0.66 | -0.31 | 0.11 | 0.08 | 0.09 | -0.06 | -0.47 | -1 | 0.2 | 0.27 | 0.14 | 0.13 | -0.03 | -0.11 | -0.1 | -0.23 | -0.81 | -0.41 | -0.47 | -0.32 | -0.5 | -0.19 | -0.24 | -0.57 | -0.63 | -0.55 | -0.02 | -0.19 | -0.33 | -1.26 | 0.23 | -0.12 | 0.27 | 0.02 | -0.07 | 0.36 | -0.06 | -0.35 | -0.13 | 0.06 | 0.52 | 0.23 | -0.06 | -0.5 | -0.28 | 0.21 | -0.03 | -0.2 | 0.3 | 0.09 | 0.02 | 0.23 | 0.72 | 0.94 | 0.56 | 0.1 | -0.23 | 0.49 | 0.22 | 0.1 | 0.54 | 0.27 | -0.49 | 0.39 | 1.33 | 1.79 | 0.98 | 0.37 | -0.23 | 0.43 | -0.06 | 0.07 | 0.41 | 0.37 | 0.12 | 0.59 | 1.72 | 1.72 | 0.71 | -0.13 | 0.01 | 0.31 | -0.08 | 0.16 | 0.7 | 0.28 | 0.09 | -0.39 | 0.62 | 1.08 | 0.97 | 0.38 | 0.36 | -0.23 | 0.09 | -0.34 | 0.27 | 0 | -0.47 | 0.2 | -0.16 | -0.25 | -0.27 | 0.09 | 1.44 | 0.74 | 0.56 | 0.62 | 0.93 | 0.01 | -1.51 | 0.03 | 0.46 | -0.15 | -0.38 | 0.13 | -0.47 | -0.28 | 0.41 | 0.05 | 0.43 | 0.2 | -0.08 | 0.02 | 0.54 | -0.15 | 0.45 | 0.09 | 0.2 | -0.2 | 0.32 | -0.02 | 0 | -0.15 | 0.19 | 0.27 | 0 | 0 | 0 | 0.05 | -0.39 | 0 | 0.2 | 0.28 | 0.03 | 0.12 | 0.42 | -0.27 | -0.61 | -0.13 | -0.03 | -0.72 | -0.48 | 0 | -0.5 | -0.1 | -0.08 | -1.06 | -0.02 | 0.2 | -1.02 | 0.55 | 0.92 | -0.75 | -2.91 | 1.19 | -0.18 | 1.89 | -0.09 | -0.22 | 0 | -1.17 | -0.15 | -1.24 | 0.68 | At1g64970 | 262875_at | G-TMT | gamma-tocopherol methyltransferase (g-TMT), nuclear; mutant is deficient in alpha and beta tocopherol; Accumulates gamma tocopherol in leaves | 10 | tocopherol O-methyltransferase activity | vitamin E biosynthesis | vitamin E biosynthesis | Plastidial Isoprenoids (Chlorophylls, Carotenoids, Tocopherols, Plastoquinone, Phylloquinone) | Tocopherol biosynthesis | tocopherol (vitamin E) biosynthesis | 1.72 | 4.79 | |||||||||||||||||||||||||
At1g56650 | 0.530 | PAP1 | Encodes a putative MYB domain containing transcription factor. Mutants are defective in the production of anthocyanin pigment. | -4.74 | -0.04 | -0.04 | -0.04 | -0.04 | -0.65 | -1.15 | -1.15 | -0.2 | -0.63 | 0.12 | -0.04 | 2.38 | -0.31 | 1.26 | 1.32 | -0.6 | -0.04 | 0.57 | 0.9 | -0.04 | -2.06 | 0.17 | -0.97 | -1.69 | 0.47 | -0.39 | 0.48 | -0.54 | -1.69 | 1.28 | 1.41 | 0.21 | -0.04 | -1.56 | -1.02 | -1.5 | -1.94 | -0.28 | -0.72 | -2.58 | -2.86 | -2.52 | 1.03 | 1.34 | -1.4 | -1.4 | -0.04 | -0.04 | -0.04 | -0.04 | -1.24 | -0.35 | -0.56 | -0.12 | 0.06 | -2.1 | -1.24 | -1.5 | -1.08 | -2.1 | -0.07 | -1.12 | -0.04 | 0.45 | -0.04 | -0.04 | -0.04 | 0.17 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 1.5 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 1.06 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 0.56 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 0.28 | 3.08 | 3.01 | 2.75 | 3.16 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 2.23 | 2.84 | 3.28 | 3.44 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 0.52 | -0.04 | 1.25 | 1.4 | 2.57 | 0.62 | 1 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -1.25 | -2.67 | -0.04 | 3.89 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.34 | -0.04 | -0.04 | 0.24 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | 0.03 | -0.04 | -0.04 | -0.04 | -0.04 | 0.19 | 1.25 | 0.18 | -0.04 | 0.1 | -0.04 | 2.36 | 2.09 | -0.78 | 1.19 | -0.04 | -0.04 | -1.49 | 1.45 | 1.09 | -1.32 | -0.04 | -0.04 | -0.04 | -0.04 | -0.04 | -3.8 | -0.04 | At1g56650 | 245628_at | PAP1 | Encodes a putative MYB domain containing transcription factor. Mutants are defective in the production of anthocyanin pigment. | 8 | Phenylpropanoid Metabolism | Flavonoid and anthocyanin metabolism | 3.96 | 8.64 | ||||||||||||||||||||||||||||
At5g07830 | 0.529 | glycosyl hydrolase family 79 N-terminal domain-containing protein, similar to beta-glucuronidase (Scutellaria baicalensis) | -0.01 | 0.09 | -0.12 | 0.02 | -0.36 | -0.78 | -0.39 | -0.22 | -0.35 | 0.06 | 0.1 | -0.07 | -0.52 | 0.08 | -0.55 | -0.53 | 0.53 | 0.59 | 0.08 | -0.09 | -0.06 | 0.53 | -0.19 | -0.03 | 0.03 | 0.08 | 0.16 | -0.18 | 0.08 | -0.05 | 0.09 | 0.34 | 0.6 | 0.04 | -0.36 | 0.13 | -0.35 | -0.56 | 0.07 | 0.05 | -0.11 | 0.12 | 0.2 | 0.08 | 0.52 | -0.1 | 0.6 | 1.02 | 1.89 | 0.82 | -0.09 | 0.05 | 0.38 | -0.04 | 0.53 | -0.49 | 0.04 | 0.07 | 0.27 | -0.3 | -0.01 | 0.22 | 0.05 | -0.23 | -0.19 | -0.3 | 0.38 | 0.14 | 0.53 | 0.47 | -0.09 | -0.07 | -0.26 | 0.31 | -0.07 | 0.07 | 0.12 | 0.14 | 0 | -0.05 | 0.06 | 0.33 | 0.22 | 0.18 | -0.09 | -0.06 | 0.06 | -0.15 | 0.05 | -0.26 | 0.13 | -0.21 | -0.02 | 0.09 | 0.83 | 0.72 | -0.08 | 0.03 | 0.15 | -0.21 | 0.07 | 0.18 | 0.4 | -0.05 | 0.61 | 1.66 | 2.52 | 2.75 | -0.25 | -0.26 | -0.19 | -0.62 | -0.3 | -0.4 | -0.05 | -0.33 | 0.07 | 0.61 | 0.85 | 1.87 | -0.34 | -0.23 | -0.49 | -0.78 | 0.04 | -0.19 | -0.35 | -0.25 | -0.42 | -0.73 | -0.04 | 0.09 | 0.6 | 0.49 | 0.06 | -0.28 | -0.31 | -0.06 | -0.06 | 0.19 | -0.26 | -0.26 | 0.39 | -0.33 | -0.65 | -0.14 | -0.34 | -0.76 | -0.94 | -0.75 | -0.85 | 0.16 | 0.08 | -0.08 | -0.17 | -0.23 | -0.48 | -0.2 | -0.7 | 0.03 | -0.24 | 0 | -0.6 | -0.94 | 0 | 0.14 | 0.31 | 0.22 | 0.11 | -0.2 | -0.33 | -0.5 | 0.05 | 0 | 0.18 | 0.09 | -1.26 | -1.69 | -1.78 | -1.02 | -0.64 | -0.03 | 0.21 | 0.02 | -0.09 | -0.4 | -0.16 | -0.19 | -0.1 | 0.2 | -0.21 | -0.14 | 0.08 | -0.86 | -0.4 | 0.73 | 1.07 | 0.99 | 0.15 | -0.14 | 0.09 | 0.37 | 0.81 | 0.33 | -2.35 | 1.61 | 0.35 | 0.61 | -0.19 | 0.09 | 0.16 | 0.3 | 0.07 | -0.79 | -0.07 | At5g07830 | 250604_at | glycosyl hydrolase family 79 N-terminal domain-containing protein, similar to beta-glucuronidase (Scutellaria baicalensis) | 1 | beta;-D-glucuronide degradation | 1.60 | 5.10 | ||||||||||||||||||||||||||||||
At1g78680 | 0.527 | GGH1 | gamma-glutamyl hydrolase (GGH1) / gamma-Glu-X carboxypeptidase / conjugase | -1.8 | -0.02 | -0.18 | -0.54 | -0.32 | -0.64 | -0.63 | -0.9 | -0.5 | -0.56 | 0.06 | 0.08 | 0.13 | -0.32 | -0.19 | 0.03 | -0.53 | -0.51 | -0.09 | -0.09 | -0.81 | -0.9 | 0.12 | -0.37 | -0.66 | -0.4 | -0.27 | 0.11 | -0.16 | -0.28 | -0.21 | 0.27 | -0.28 | -0.16 | -0.55 | -0.5 | -0.31 | -0.15 | -0.13 | -0.35 | -0.68 | -1.05 | -1.14 | -0.05 | -0.2 | -0.25 | -0.52 | -0.98 | -1.17 | -0.08 | -0.2 | -0.12 | 0.04 | -0.35 | -0.33 | -0.06 | -1.11 | 0.02 | -1.03 | -0.28 | -0.85 | 0.11 | -0.35 | 0.26 | -0.15 | 0.36 | 0.22 | -0.15 | -0.24 | -0.28 | 0.67 | 0.12 | 0.19 | 0.35 | 0.73 | 0.6 | 0.28 | -0.86 | 0.14 | 0.07 | 0.77 | 0.34 | 0.34 | 0.48 | 0.19 | 0.08 | 0.13 | 0.06 | 0.05 | 0.56 | 0.31 | 0.07 | 0.49 | 0.49 | 0.6 | 0.21 | -0.01 | 0.24 | 0.3 | 0.27 | 0.24 | 0.28 | -0.01 | 0.24 | 1.61 | 1.18 | 0.69 | 1.26 | 0.02 | 0.92 | 1.41 | 1.1 | 1.31 | 1.23 | 0.09 | 0.43 | 1.85 | 1.23 | 1.3 | 1.12 | 0.22 | 0.68 | 0.7 | 0.38 | 1.2 | 0.65 | 0.25 | 0.04 | 1.33 | 0.93 | 1.44 | 0.73 | 0.24 | 0.42 | 0.08 | -0.15 | 0.06 | 0.26 | 0.02 | 0.04 | 0.06 | -0.53 | 0.77 | -0.36 | -0.47 | 0.45 | -0.47 | -1.31 | -1.58 | -1.66 | -1.52 | -0.28 | -0.25 | -0.12 | -0.27 | -0.4 | -0.79 | -0.14 | 0.66 | -0.51 | 0.54 | 0.65 | -0.02 | -0.79 | -0.17 | -0.17 | -0.1 | 0.24 | 0.47 | -0.02 | 0.12 | 0.46 | 1.19 | 0.67 | 1.03 | 0.44 | -0.34 | -0.47 | -1.21 | 0.54 | 0.52 | 0.38 | 0.03 | 0 | 0.01 | -0.1 | 0.2 | 0.1 | 0.28 | 0.48 | 0.28 | -0.09 | 0.26 | -0.74 | -1.28 | -1.33 | -0.82 | -0.91 | 0.7 | 0.6 | -0.31 | -0.48 | 0.34 | -1.35 | -2.81 | 2.06 | 0.7 | 0.56 | 0.28 | -0.13 | -0.08 | -0.36 | 0.01 | -2.47 | -0.05 | At1g78680 | 264250_at | GGH1 | gamma-glutamyl hydrolase (GGH1) / gamma-Glu-X carboxypeptidase / conjugase | 6 | Folate biosynthesis | 2.39 | 4.88 | ||||||||||||||||||||||||||||
At4g13010 | 0.526 | oxidoreductase, zinc-binding dehydrogenase family protein | -1.99 | 0.15 | 0.11 | 0.16 | -0.43 | -0.8 | -0.54 | -0.56 | -0.69 | -0.54 | -0.17 | -0.09 | 0.28 | -0.51 | -0.32 | 0.01 | -0.13 | -0.47 | -0.25 | -0.13 | -0.67 | -0.19 | -0.1 | -0.04 | 0.02 | 0 | -0.2 | 0.22 | 0 | -0.13 | -0.17 | -0.07 | -0.39 | -0.16 | -0.3 | -0.2 | -0.18 | -0.12 | -0.14 | -0.04 | -0.22 | -0.32 | -0.19 | -0.3 | -0.79 | 0.02 | -0.12 | -0.28 | 0.05 | -0.18 | 0.04 | -0.05 | 0.13 | -0.09 | 0.19 | -0.24 | -0.23 | -0.37 | -0.32 | -0.32 | -0.12 | -0.11 | 0.04 | -0.06 | -0.17 | 0.13 | 0.13 | -0.37 | -0.03 | -0.2 | 0.04 | -0.25 | -0.12 | -0.22 | 0.08 | 0.32 | -0.28 | 0.47 | -0.14 | -0.02 | 0.07 | 0.24 | 0.09 | 0.05 | -0.36 | -0.15 | 0.11 | 0.05 | 0.01 | -0.02 | -0.2 | 0.13 | 0.14 | 0.38 | 0.3 | 0.17 | -0.36 | -0.3 | -0.16 | -0.2 | -0.08 | -0.16 | -0.17 | -0.04 | 0.37 | 0.98 | 1.05 | 0.85 | -0.31 | 0.2 | 0.2 | 0.14 | 0.64 | 0.3 | -0.2 | 0.17 | 0.21 | 0.75 | 0.69 | 0.35 | -0.06 | 0.01 | 0.04 | 0.4 | 0.26 | 0.06 | -0.17 | -0.13 | 0.13 | 0.18 | 0.04 | 0.24 | 0.03 | 0.15 | 0.31 | -0.15 | 0.1 | -0.15 | -0.14 | -0.07 | -0.48 | -0.03 | -0.19 | -0.03 | 0.31 | 0.17 | -0.06 | -0.09 | 0.49 | 1.38 | -0.17 | -0.01 | 0.11 | 0.17 | 0.33 | 0.49 | -0.04 | 0.25 | 0.16 | -0.82 | 0.16 | 0.14 | 0.08 | 0.19 | -0.01 | 0.1 | 0.52 | 0.21 | 0.21 | -0.4 | -0.23 | 0.27 | 0.79 | -0.14 | 0.34 | -0.05 | 0.26 | 0.46 | 0.84 | 1.18 | 1.07 | 0.95 | -0.09 | -0.24 | -0.13 | -0.16 | 0.54 | 0.27 | 0.06 | -0.06 | 0.06 | -0.21 | -0.03 | 0.05 | -0.24 | 0.03 | 0.15 | -0.1 | -0.66 | 0.28 | -0.38 | 0.01 | -0.18 | 0.17 | -2 | 0.48 | 0.25 | 0.67 | -0.22 | 0.09 | 0.28 | -0.28 | 0.16 | 0.53 | -0.74 | At4g13010 | 254804_at | oxidoreductase, zinc-binding dehydrogenase family protein | 2 | threonine degradation | 1.22 | 3.39 | ||||||||||||||||||||||||||||||
At3g08860 | 0.521 | alanine--glyoxylate aminotransferase, putative / beta-alanine-pyruvate aminotransferase, putative | -0.92 | -0.41 | -0.86 | -1.42 | -0.41 | -1.03 | -1.03 | -1.03 | 0.37 | -0.63 | -0.41 | -0.67 | 3.77 | -0.12 | 0.41 | 3.15 | -0.41 | -0.67 | 0.09 | -0.41 | -0.67 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | 0.73 | 0.2 | -0.41 | -1.25 | -0.41 | -0.41 | -0.41 | -0.41 | -0.7 | -1.3 | -1.1 | -0.36 | 2.98 | 3.32 | -0.77 | -2.52 | -0.41 | -0.41 | -0.41 | -1.32 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.21 | -0.41 | -0.41 | 0.37 | -0.41 | 0.06 | -0.51 | -0.36 | -0.14 | 0.49 | -0.44 | 0.68 | -1.07 | 1.03 | 0.33 | -0.41 | -0.41 | 0.09 | 0.11 | -0.34 | 0.73 | 0.15 | 0.84 | -0.5 | 0.26 | 1.28 | 1.61 | -0.23 | -0.41 | -0.2 | 0.62 | 0.49 | -0.26 | -0.01 | 1.01 | -0.39 | 1.36 | 1.15 | 1.24 | -0.41 | -0.41 | 2.74 | 4.26 | 3.83 | 3.84 | -0.5 | 0.51 | 1.05 | 3.06 | 3.5 | 3.83 | -0.35 | -0.41 | 3.35 | 4.18 | 2.96 | 3.91 | -0.53 | 0.06 | 0.18 | 0.52 | 2.87 | 2.06 | -0.09 | -0.41 | -0.41 | -0.41 | 1.21 | 0.84 | 0.72 | 0.63 | -1.29 | -1.03 | -0.04 | 0.08 | 1.67 | -0.48 | 0.13 | -0.41 | 2.43 | -0.41 | 0.26 | -0.41 | -0.41 | -0.41 | -0.41 | -1.1 | -1.78 | -1.25 | 0 | -0.17 | 0.63 | -1.04 | -1.52 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -0.41 | -1.6 | -0.41 | -1.1 | -1.03 | -0.48 | 0.71 | -0.33 | -1.12 | 0.72 | 0.26 | 2.25 | 0.62 | -0.09 | 0.2 | -0.41 | -1.31 | -1.11 | -0.41 | -0.52 | -0.6 | -1.52 | 0.09 | -0.4 | -1.46 | -0.59 | 0.22 | -0.68 | -0.06 | -0.02 | -0.41 | -0.41 | -0.41 | -0.72 | -1.78 | -0.41 | -0.41 | -0.41 | 0.85 | -0.76 | -2.57 | -5.13 | 3.19 | 1.07 | -0.41 | 0.43 | -0.89 | -0.87 | -3.17 | -0.41 | -1.36 | -0.41 | At3g08860 | 258983_at | alanine--glyoxylate aminotransferase, putative / beta-alanine-pyruvate aminotransferase, putative | 4 | chlorophyll biosynthesis | biosynthesis of proto- and siroheme | biotin biosynthesis I | arginine degradation II | arginine degradation III | arginine degradation V | glutamate degradation I | 4.54 | 9.40 | ||||||||||||||||||||||||||||||
At1g73680 | 0.518 | similar to pathogen-inducible alpha-dioxygenase (Nicotiana attenuata) | -2.58 | 0.15 | -0.11 | -0.8 | -0.36 | -0.46 | -0.02 | -0.4 | -0.7 | -0.3 | -0.52 | -0.44 | 0.11 | -0.23 | -0.72 | -0.07 | -0.67 | 0.07 | 0.13 | -0.5 | -0.48 | 0.36 | 0.01 | -0.16 | 0.12 | -0.19 | -0.17 | -0.09 | -0.41 | 0.13 | -0.36 | -0.21 | 0.22 | -0.03 | -0.51 | 0.14 | -0.01 | 0.11 | 0.1 | -0.11 | -0.34 | -0.06 | 0.16 | 0 | -0.45 | 0.03 | -0.56 | -0.28 | -0.28 | 0.44 | -0.42 | -0.41 | 0.26 | -0.41 | 0.28 | -0.55 | -0.22 | -0.38 | -0.28 | -0.51 | 0.59 | -0.1 | 0 | -0.56 | -0.67 | -0.86 | -0.26 | 0.37 | 0.17 | 0.45 | -0.04 | -0.2 | -0.42 | -0.33 | -0.2 | 0.24 | 0.28 | -0.42 | 0.06 | -0.03 | -0.04 | 0.56 | -0.11 | -0.05 | -0.07 | -0.31 | 0.31 | -0.16 | -0.2 | 0.15 | -0.26 | 0.27 | -0.25 | 0.51 | 0.1 | 0.06 | -0.12 | -0.24 | 0.56 | 0.61 | 0.3 | -0.16 | -0.04 | -0.09 | 0.92 | 2.25 | 1.96 | 2.45 | 0.08 | -0.52 | 0.72 | 1.45 | 1.69 | 1.91 | -0.12 | 0.23 | 0.46 | 1.26 | 0.42 | 1.35 | 0.18 | -0.09 | 0.32 | 0.2 | 1.5 | 1.38 | -0.07 | -0.27 | -0.28 | 0 | -0.03 | 0.72 | 0.02 | 0.16 | -0.18 | -0.15 | -0.75 | -0.05 | -0.28 | -0.09 | -0.54 | -0.33 | 0.03 | -0.37 | -0.85 | -0.25 | 0.14 | -0.26 | 0.06 | -0.73 | -0.18 | 0.34 | 0.16 | 0.08 | 0.35 | -0.17 | -0.14 | -0.54 | -0.26 | -0.27 | 0.11 | -0.47 | -0.07 | -0.52 | -0.28 | 0.03 | -0.15 | 0.05 | 0.35 | 0.08 | 0.03 | 1.28 | 0.78 | 0.31 | 0.47 | 0.03 | -0.01 | -0.01 | -0.01 | -0.01 | -0.01 | -0.01 | -0.01 | -0.01 | -0.09 | 0.6 | -0.49 | 0.26 | 0.11 | 0.61 | 0.64 | -0.21 | 0.2 | 0.03 | -1.08 | -0.12 | -0.1 | -0.1 | 0.05 | 0.59 | -0.12 | 0.57 | -0.35 | -0.42 | -2.65 | 0.67 | -0.08 | 1.54 | 0.15 | 0.27 | 0.23 | -0.68 | -0.34 | -1.82 | -0.32 | At1g73680 | 260060_at | similar to pathogen-inducible alpha-dioxygenase (Nicotiana attenuata) | 4 | Lipid signaling | 1.95 | 5.09 | ||||||||||||||||||||||||||||||
At3g48000 | 0.515 | ALDH2B4 | putative (NAD+) aldehyde dehydrogenase | -0.5 | 0.1 | -0.07 | -0.3 | 0.04 | 0.09 | 0.14 | 0.21 | 0.23 | 0.51 | 0.11 | -0.05 | 0.72 | -0.2 | -0.48 | 0.74 | 0.15 | 0.23 | 0.69 | 0.09 | 0.19 | 0.62 | -0.11 | -0.18 | -0.27 | -0.04 | -0.24 | -0.09 | -0.14 | -0.21 | -0.28 | -0.01 | -0.08 | -0.22 | -0.22 | -0.01 | -0.01 | 0.09 | -0.1 | 0.08 | -0.2 | -0.19 | -0.3 | 0.24 | 0.35 | -0.34 | -0.3 | 0.01 | 0.24 | 0.05 | -0.05 | 0.04 | 0.21 | -0.1 | 0.18 | -0.08 | 0.46 | -0.03 | 0.39 | 0.07 | 0.37 | 0.04 | 0.23 | -0.12 | -0.36 | -0.38 | 0.42 | 0.45 | 0.46 | 0.52 | 0.02 | -0.13 | 0.33 | 0 | 0.27 | -0.01 | 0.19 | 0.33 | -0.23 | -0.13 | -0.15 | -0.13 | -0.28 | -0.2 | -0.24 | 0.28 | -0.03 | 0.04 | -0.06 | 0.13 | -0.37 | -0.19 | -0.09 | -0.05 | -0.02 | -0.04 | -0.16 | 0.25 | -0.05 | -0.11 | 0.06 | 0.28 | 0.03 | -0.25 | 0.14 | 0.79 | 1.02 | 1.58 | -0.31 | 0.11 | -0.03 | 0.43 | 0.65 | 0.93 | -0.24 | -0.16 | 0.04 | 0.36 | 0.27 | 0.68 | -0.28 | 0.17 | -0.2 | -0.36 | 0.23 | 0.46 | -0.21 | -0.15 | -0.32 | -0.18 | 0.21 | 0.54 | 0.23 | 0.13 | -0.04 | -0.32 | -0.16 | -0.44 | 0.25 | 0.11 | 0.08 | -0.15 | 1.05 | -0.13 | -0.06 | -0.41 | -0.23 | -0.32 | -0.28 | -0.09 | -0.63 | -0.19 | 0.19 | -0.07 | -0.23 | -0.45 | -0.94 | -0.41 | 0.19 | 0.49 | -0.02 | -0.28 | -0.21 | -0.88 | -0.36 | 0.03 | -0.11 | -0.13 | 0.04 | -0.21 | 0.2 | -0.75 | -0.56 | 0.04 | 0.1 | 0.02 | -0.02 | -0.17 | -0.38 | -0.78 | -0.68 | -0.48 | -0.23 | -0.05 | 0.18 | -0.11 | 0.21 | -0.52 | 0.24 | 0.06 | 0.44 | 0.11 | 0.09 | -0.46 | -0.07 | 0.28 | 0.01 | -0.02 | -0.55 | 0.3 | -0.1 | 0.41 | 0.27 | 0.27 | -1.85 | 0.26 | -0.07 | 0.97 | -0.23 | 0.28 | 0.35 | 0.09 | 0.02 | -0.89 | -0.28 | At3g48000 | 252372_at | ALDH2B4 | putative (NAD+) aldehyde dehydrogenase | 8 | energy conversion and regeneration | arginine degradation IX | 4-hydroxyproline degradation | proline degradation I | proline degradation II | Glycolysis / Gluconeogenesis | Ascorbate and aldarate metabolism | Pyruvate metabolism | Propanoate metabolism | Butanoate metabolism | Fatty acid metabolism | Bile acid biosynthesis | Glycerolipid metabolism | Valine, leucine and isoleucine degradation | Lysine degradation | Arginine and proline metabolism | Histidine metabolism | Tryptophan metabolism | beta-Alanine metabolism | Limonene and pinene degradation | 1,2-Dichloroethane degradation | Intermediary Carbon Metabolism | Aldehyde dehydrogenase, Family 2: class-1/2 ALDHs | 1.13 | 3.43 | ||||||||||||||||||||||||
At1g12050 | 0.513 | Similar to fumarylacetoacetase (Fumarylacetoacetate hydrolase, Beta-diketonase, FAA) from Rattus norvegicus | -0.39 | -0.17 | -0.01 | 0.25 | -0.19 | -0.71 | -0.75 | -0.22 | -0.45 | 0.03 | -0.35 | -0.15 | 0.63 | -0.21 | -0.7 | 0.3 | -0.37 | -0.01 | 0.5 | -0.08 | -0.39 | 0.46 | 0.11 | -0.15 | -0.01 | 0.41 | -0.31 | 0.07 | -0.11 | -0.04 | 0.45 | 0.26 | -0.44 | 0.01 | -0.35 | 0.11 | -0.05 | -0.04 | 0.13 | 0.27 | -0.37 | -0.44 | -0.46 | 0.08 | 0.41 | -0.28 | 0.05 | -0.48 | 0.55 | 0.68 | -0.16 | 0.05 | 0.14 | 0.05 | -0.06 | 0.05 | -0.76 | 0.05 | -0.88 | 0.05 | -0.72 | 0.05 | -0.26 | 0.15 | -0.02 | -0.93 | -0.13 | -0.11 | 0.13 | 0.24 | 0.02 | 0.18 | -0.07 | -0.19 | 0.11 | -0.8 | -0.03 | 0.14 | 0.1 | -0.24 | 0 | 0.22 | 0.21 | -0.06 | 0.22 | 0.35 | -0.54 | -0.12 | 0.07 | 0.09 | 0.3 | 0.01 | 0.1 | 0.21 | 0.24 | 0.14 | 0.3 | 0.26 | -0.09 | 0.07 | -0.08 | 0.09 | 0.18 | -0.32 | 0.26 | 1.22 | 0.9 | 0.74 | 0.12 | 0.05 | 0.16 | 0.48 | -0.2 | 0.34 | 0.28 | 0.25 | 0.43 | 0.85 | 0.85 | 1.1 | 0.3 | -0.09 | -0.28 | -0.36 | -0.02 | 0.08 | 0.27 | -0.04 | 0.22 | -0.06 | 0.24 | 0.47 | 0.42 | 0.34 | -0.16 | 0.18 | 0.03 | -0.01 | 0.81 | 0.18 | 0.24 | -0.21 | 0.72 | 0.05 | 0.25 | 0.4 | -0.41 | -0.7 | -0.54 | -0.47 | -0.26 | -0.09 | -0.28 | -0.17 | -0.53 | -0.73 | -0.52 | -0.61 | 0.44 | 0.54 | 0.48 | 0.41 | -0.09 | -0.9 | -0.16 | -0.04 | 0.15 | 0.31 | 0.34 | 0.23 | 0.01 | -1.08 | -0.08 | 0.5 | 0.81 | 0.71 | -0.21 | -0.49 | -0.83 | -1.27 | -1.07 | -0.96 | -0.22 | -0.35 | -0.18 | 0.21 | 0.3 | 1.12 | 0.43 | 0.27 | -0.2 | -0.07 | -0.08 | -0.39 | -0.47 | 0.09 | 0.39 | 0.05 | 0.35 | 0.08 | -0.15 | 0.07 | 0.89 | -0.49 | -2.77 | 0.78 | -0.11 | 1.51 | -0.28 | 0.14 | 0.23 | -0.09 | -0.1 | -0.41 | 0.16 | At1g12050 | 264396_at | Similar to fumarylacetoacetase (Fumarylacetoacetate hydrolase, Beta-diketonase, FAA) from Rattus norvegicus | 2 | phenylalanine degradation I | tyrosine degradation | Tyrosine metabolism | Styrene degradation | 1.50 | 4.29 | |||||||||||||||||||||||||||||
At1g68530 | 0.512 | CUT1 | very-long-chain fatty acid condensing enzyme (CUT1); required for cuticular wax biosynthesis and pollen fertility; involved in wax biosynthesis; required for elongation of C24 very-long-chain fatty acids | -4.62 | 0.28 | 0 | -0.41 | -0.23 | -0.5 | -0.15 | -0.21 | -1.07 | -0.84 | -0.36 | -0.22 | -0.98 | -0.35 | -0.09 | -0.96 | -0.12 | -0.07 | -0.6 | 0 | -0.74 | -1.25 | 0.13 | 0.11 | -0.34 | -0.19 | -0.03 | 0.12 | 0.12 | -0.12 | -0.31 | -0.05 | -0.02 | -0.14 | -1.19 | 0.18 | 0.27 | 0.36 | 0.05 | 0.05 | -0.34 | -0.79 | -0.7 | -0.18 | -0.87 | -0.01 | 0.82 | -0.77 | -0.02 | -0.33 | -0.26 | 0.34 | 0.56 | 0.04 | 0.32 | -0.1 | -0.42 | 0.03 | -0.72 | -0.12 | 0.56 | 0.54 | 0.46 | -0.02 | -0.21 | 0.21 | 0.23 | -0.04 | 0.24 | 0.43 | -0.73 | -0.04 | 1.29 | 0.26 | 0.15 | -1.02 | -0.28 | -0.42 | 0.28 | 0.3 | 0.26 | 0.37 | 0.39 | 0.6 | 0.11 | 1.38 | 0.02 | 0.15 | 0.66 | 0.57 | 0.07 | 0.57 | 0.25 | 0.22 | 0.4 | 0.33 | 0.16 | 1.45 | -0.71 | 0.56 | -0.13 | -0.66 | 0.31 | 0.11 | 1.43 | 1.67 | 1.77 | 1.66 | -0.01 | 1.46 | 1.56 | 2.25 | 1.25 | 0.78 | 0.21 | 0.23 | 1.22 | 1.32 | 1.13 | 1.66 | 0.17 | 1.95 | 0.53 | 0.91 | 1.19 | -0.38 | 0.37 | -0.08 | 0.47 | 0.21 | 0.98 | 0.38 | 0.45 | 0.56 | -0.42 | 0.03 | 1.99 | 0.32 | 0.34 | -0.3 | -0.51 | 0.53 | 1.38 | -0.52 | -1.27 | -0.1 | -0.03 | -0.02 | -0.39 | -1.1 | -0.93 | -0.31 | 0.78 | -0.7 | 0.15 | 0.08 | -0.28 | -0.26 | -1.99 | 0.11 | -0.09 | 0.24 | 0.38 | 0.12 | -0.95 | -0.42 | -0.26 | 0.02 | -0.61 | 0.15 | 0.81 | 0.51 | 0.96 | -0.4 | -0.21 | -0.52 | -0.49 | -0.62 | -0.69 | -0.06 | 0.57 | -1.14 | -1.97 | -1.29 | -0.84 | -0.97 | 1.56 | -1.11 | -0.56 | -0.6 | -1.45 | -0.35 | -0.02 | -1.13 | -1.25 | -1.34 | -0.42 | 0.05 | 0.28 | 0.87 | 0.28 | -0.08 | -0.92 | -0.31 | -4.2 | 1.73 | 0.92 | 1.42 | 0.13 | 0.16 | 0.44 | 0.37 | 0.11 | -2.54 | 0.11 | At1g68530 | 260267_at | CUT1 | very-long-chain fatty acid condensing enzyme (CUT1); required for cuticular wax biosynthesis and pollen fertility; involved in wax biosynthesis; required for elongation of C24 very-long-chain fatty acids | 8 | very-long-chain fatty acid metabolism | cuticle biosynthesis | wax biosynthesis | epicuticular wax biosynthesis | acetyl-CoA assimilation | glyoxylate cycle | TCA cycle variation IV | TCA cycle -- aerobic respiration | serine-isocitrate lyase pathway | TCA cycle variation VIII | Fatty acid elongation and wax and cutin metabolism | 2.66 | 6.88 | ||||||||||||||||||||||||||
At1g07250 | 0.510 | UDP-glucoronosyl/UDP-glucosyl transferase family protein | -1.15 | 0.31 | 0.15 | 0.43 | -0.24 | -0.72 | -0.67 | -0.49 | -0.18 | -0.36 | -0.08 | -0.07 | -0.01 | -0.31 | -0.18 | -0.47 | -0.09 | -0.22 | -0.64 | -0.23 | -0.65 | -0.7 | -0.01 | -0.12 | -0.44 | -0.1 | 0.14 | 0.03 | 0.08 | -0.6 | -0.35 | -0.06 | -0.63 | 0.15 | -0.06 | 0.2 | 0.18 | 0.25 | 0.11 | 0.22 | -0.13 | -0.21 | -0.56 | -0.14 | -0.3 | 0.03 | -0.7 | -0.34 | -0.08 | 0 | -0.39 | 0.04 | 0.15 | -0.05 | 0.14 | -0.55 | -0.26 | -0.47 | -0.1 | -0.57 | -0.14 | 0.12 | 0.32 | -0.37 | -0.28 | 0.09 | -0.03 | 0.03 | 0.19 | 0.39 | -0.01 | 0.12 | 0.15 | 0.28 | 0.31 | -0.28 | 0.12 | -0.04 | 0.07 | 0.14 | 0.26 | 0.08 | -0.18 | -0.24 | 0.12 | 0.14 | 0.1 | 0.04 | 0.04 | 0.33 | 0.51 | 0.43 | 0.19 | 0.27 | -0.12 | 0.03 | 0.34 | 0.24 | 0.15 | 0.15 | 0.23 | 0.34 | 0.04 | 0.16 | 0.57 | 0.93 | 1.03 | 0.97 | -0.1 | 0.04 | 0.51 | 0.78 | 0.52 | 0.63 | 0.45 | 0.16 | 0.57 | 0.42 | 0.43 | 0.53 | -0.18 | -0.23 | -0.65 | -1.49 | 0.25 | 0.11 | 0.2 | 0.05 | 0.27 | -0.15 | 0.3 | 0.31 | 0.11 | 0.24 | -0.19 | -0.57 | -0.16 | 0.16 | 0.28 | 0 | 0.01 | -0.81 | 0.24 | 0.14 | 0.37 | 0.1 | -0.17 | -0.22 | -0.09 | 0.22 | -0.75 | 0.33 | 0.24 | 0.27 | 0.05 | -0.56 | -0.45 | -0.82 | -0.96 | 0.11 | -0.16 | -0.28 | -1.1 | -0.98 | -0.3 | -0.18 | -0.01 | 0.12 | -0.04 | 0.18 | -0.15 | -0.8 | 0.22 | 0.5 | 0.09 | 0.06 | -0.05 | -0.23 | -0.23 | 0 | 0.42 | -0.24 | -0.4 | -0.01 | 0.24 | 0.73 | 0.91 | 0.78 | 0.3 | 0.07 | 0.55 | 0.23 | 0.98 | 1.24 | -0.22 | -0.52 | -0.26 | -0.14 | 0.25 | 0.65 | 0.26 | -0.21 | -0.46 | 0.11 | -1.38 | 0.92 | 1.02 | 0.4 | -0.07 | 0.52 | 0.26 | -0.63 | -0.03 | -0.14 | 0.21 | At1g07250 | 256033_at | UDP-glucoronosyl/UDP-glucosyl transferase family protein | 1 | Glycosyl transferase, Family 1 | 1.38 | 2.73 | ||||||||||||||||||||||||||||||
At3g52880 | 0.504 | similar to monodehydroascorbate reductase (NADH), Lycoperison esculentum | -0.2 | -0.09 | -0.15 | 0.27 | 0.1 | 0.01 | 0.05 | 0.19 | -0.19 | -0.03 | 0.1 | -0.22 | -0.27 | 0.1 | -0.1 | 0.04 | -0.05 | -0.1 | -0.2 | 0.01 | -0.21 | -0.31 | -0.13 | -0.08 | 0.04 | 0.3 | -0.22 | -0.22 | -0.03 | 0.07 | -0.04 | -0.18 | 0.06 | -0.03 | 0.21 | -0.06 | -0.11 | -0.21 | 0.14 | 0.07 | 0 | -0.01 | 0.34 | 0.24 | 0.34 | -0.02 | 0.04 | 0.01 | 0.12 | 0.32 | -0.3 | 0.1 | -0.24 | -0.19 | -0.15 | -0.26 | -0.25 | -0.1 | -0.36 | -0.13 | -0.24 | -0.06 | -0.23 | -0.23 | 0.23 | -0.13 | 0.07 | -0.28 | 0.13 | -0.04 | -0.27 | 0.45 | 0.18 | -0.18 | 0.17 | -0.35 | -0.1 | 0.27 | -0.05 | -0.23 | 0.03 | -0.18 | 0.02 | -0.47 | 0.28 | 0.15 | -0.54 | -0.05 | -0.02 | -0.17 | -0.05 | -0.3 | 0.26 | 0.23 | 0.56 | 0.06 | 0.09 | 0.3 | -0.15 | 0.84 | 0.62 | 0.69 | 0.26 | -0.13 | 0.02 | 0.2 | 0.36 | 0.07 | 0.18 | 0.08 | -0.12 | 0.54 | 0.39 | 0.27 | -0.01 | -0.19 | 0.31 | 0.39 | 0.5 | -0.11 | -0.05 | -0.15 | -0.55 | -0.49 | 0.17 | 0.14 | 0.12 | -0.11 | 0.22 | -0.15 | 0.26 | -0.11 | 0.15 | -0.31 | -0.38 | 0.13 | 0.12 | 0.14 | 0.62 | -0.09 | -0.13 | -0.2 | -0.02 | 0.45 | 0.09 | 0.35 | -0.06 | -0.02 | -0.02 | 0.02 | -0.71 | 0 | 0.13 | -0.39 | 0.23 | -0.04 | -0.05 | 0.06 | 0.38 | 0.18 | 0.23 | 0.45 | -0.04 | 0.07 | 0.07 | -0.27 | 0.52 | -0.04 | -0.31 | 0.07 | 0.05 | -0.83 | -0.12 | 0.12 | 0.32 | 0.25 | -0.16 | -0.06 | -0.11 | -0.53 | -0.45 | -0.53 | -0.04 | -0.03 | -0.47 | -0.04 | 0.1 | 0.01 | 0.28 | -0.06 | -0.35 | -0.16 | 0.01 | -0.36 | 0.07 | 0.16 | 0.35 | 0 | -0.21 | 0.01 | -0.43 | 0.15 | 0.87 | 0.19 | -4.63 | 1.57 | 0.43 | 1.38 | 0.45 | -0.2 | -0.06 | -0.36 | -0.18 | 0.81 | -0.07 | At3g52880 | 252024_at | similar to monodehydroascorbate reductase (NADH), Lycoperison esculentum | 4 | biosynthesis of vitamins, cofactors, and prosthetic groups | stress response | Cell Wall Carbohydrate Metabolism | ascorbic acid biosynthesis | 0.94 | 6.20 | |||||||||||||||||||||||||||||
At1g07720 | 0.503 | beta-ketoacyl-CoA synthase family protein | -3.22 | -0.37 | -0.37 | -0.48 | -0.74 | -1.21 | -1.05 | -1.02 | -1.09 | -1.29 | -1.03 | -0.65 | 0.43 | -1.03 | 0.74 | -1.11 | -1.09 | -1.12 | -1.06 | -0.64 | -1.25 | -1.22 | 0.18 | 0.56 | -0.3 | 0.13 | -0.3 | 0.65 | 0.36 | -0.48 | 0.26 | 0.05 | -0.33 | -0.46 | -1.51 | -0.08 | -0.02 | 0.09 | 0.05 | 0.09 | -0.42 | -1.11 | -1.01 | 0.13 | -0.66 | -0.07 | 0.83 | -0.94 | -0.3 | -0.57 | -0.46 | -0.03 | 0.23 | -0.37 | 0.06 | -0.99 | -1.03 | -0.52 | -1.12 | -1.24 | -0.06 | 0.07 | 0.35 | 0.61 | 0.12 | -0.28 | -0.06 | -0.37 | -0.08 | -0.18 | -0.6 | 0.15 | 0.65 | -0.1 | 0.13 | -0.76 | 0.28 | 0.56 | 0.42 | -0.3 | -0.17 | 0.17 | 0.47 | 0.32 | 0.23 | 1.15 | -0.27 | -0.11 | 0.26 | 0.53 | -0.32 | 0.07 | 0 | 0.11 | 0.28 | 0.06 | 0.21 | 1.34 | -0.3 | 0.15 | -0.34 | -0.46 | -0.34 | -0.34 | 2.25 | 2.94 | 3.43 | 3.62 | 0.43 | 1.77 | 0.73 | 1.47 | 1.47 | 1.09 | -0.47 | -0.49 | 2.06 | 2.1 | 1.94 | 2.52 | 0.24 | 1.19 | 0.54 | 0.31 | 1.52 | 0.33 | 0.28 | -0.05 | 0.69 | 0.24 | 0.31 | -0.23 | 0.25 | 0.33 | -0.42 | 0.27 | 1.37 | -0.1 | 0.24 | -0.08 | 0.06 | 2.02 | 1.08 | 0.65 | 0.25 | -0.11 | -0.19 | 0.5 | 0.26 | -0.63 | 0.95 | -0.19 | 0.92 | -0.23 | 0.69 | 0.65 | 0.31 | -1.28 | -1.88 | 0.07 | 0.31 | 0.04 | -1.25 | 0.13 | -0.81 | 0.36 | 0.18 | 0.18 | -0.45 | 0.31 | 0.66 | 0.11 | 0.16 | 0.22 | 0.18 | 0.14 | -0.56 | -0.59 | -0.44 | 0.88 | 1.69 | -0.31 | -1.57 | -0.84 | -0.57 | -0.43 | 1.35 | -0.69 | -0.28 | -0.3 | -0.74 | -0.4 | -0.56 | -1.51 | -1.41 | -0.91 | -0.28 | -0.44 | 0.54 | 0.37 | 0.31 | 0.19 | -0.5 | -1.02 | -2.54 | 1.03 | 1.39 | 0.15 | 0.62 | -0.04 | 0.43 | 0.33 | 0.07 | -3.67 | 0.07 | At1g07720 | 261420_at | beta-ketoacyl-CoA synthase family protein | 4 | fatty acid elongation -- saturated | fatty acid biosynthesis -- initial steps | fatty acid elongation -- unsaturated | Fatty acid elongation and wax and cutin metabolism | 2.82 | 7.29 | |||||||||||||||||||||||||||||
At3g51830 | 0.503 | ATG5 | contains similarity to phosphoinositide phosphatase SAC1 (Rattus norvegicus); putative transmembrane protein G5p (AtG5) | -0.7 | -0.26 | -0.28 | -0.76 | -0.13 | -0.54 | -0.5 | -0.66 | -0.72 | -0.26 | 0.06 | -0.93 | 0.16 | -0.14 | -0.25 | -0.33 | -0.01 | -0.35 | -0.37 | 0.18 | -0.69 | -0.41 | -0.34 | 0.26 | -0.16 | 0.19 | -0.05 | 0.05 | 0.18 | -0.3 | 0.28 | -0.18 | -0.37 | -0.03 | 0.13 | 0.07 | 0.13 | 0.01 | 0.16 | 0.22 | -0.19 | -0.51 | -0.63 | -0.21 | 0.08 | -0.04 | 0.13 | -0.27 | 0.22 | 0.22 | 0.02 | 0.14 | 0.12 | 0.2 | 0.33 | -0.18 | -0.17 | 0.33 | -0.31 | 0.09 | -0.46 | 0.27 | -0.03 | -0.32 | -0.51 | -0.28 | 0.12 | 0.01 | -0.21 | -0.16 | 0.4 | -0.07 | 0.2 | 0.16 | 0.34 | 0.11 | -0.27 | -0.32 | -0.24 | 0.06 | 0.44 | 0.66 | 0.47 | -0.04 | 0.22 | 0.27 | 0.02 | 0.09 | 0.09 | 0.12 | 0.45 | 0.61 | 0.22 | 0.95 | 0.66 | 0.18 | 0.24 | 0.33 | 0.28 | 0.3 | 0 | -0.1 | -0.37 | 0.31 | 0.98 | 1.49 | 1.56 | 1.79 | -0.16 | 0.2 | 0.45 | 0.3 | 0.57 | 0.22 | -0.23 | 0.69 | 1.19 | 0.78 | 0.84 | 0.82 | -0.12 | 0.15 | 0.16 | 0.07 | 0.45 | 0.02 | 0.15 | -0.3 | 0.02 | 0.55 | 0.56 | 0.43 | 0.15 | 0.07 | -0.14 | -0.27 | -0.16 | 0.18 | 0.18 | 0.1 | -0.13 | -0.38 | 0.99 | -0.6 | -0.36 | 0.04 | 0.42 | -0.66 | -0.67 | -0.45 | -1.23 | -0.32 | -0.06 | 0.23 | -0.28 | -0.5 | -1 | -0.3 | 0.11 | -0.3 | 0.26 | 0.21 | 0.38 | -0.13 | 0.42 | 0.51 | 0.69 | 0.11 | 0.27 | -0.13 | -0.27 | -0.89 | 0.53 | 0.07 | 0.73 | 0.38 | -0.02 | -0.48 | -0.77 | -0.93 | -0.55 | -0.15 | -0.16 | -0.18 | -0.35 | -0.2 | 0.17 | -0.27 | -0.12 | 0 | 0.12 | -0.12 | -0.23 | -0.08 | -0.91 | -0.31 | -0.15 | -0.18 | 0.1 | 0.31 | -0.02 | -0.22 | -0.45 | -0.42 | -2.87 | 0.95 | -0.22 | 0.91 | -0.1 | -0.57 | -0.12 | -0.6 | -0.03 | 0.08 | 0.72 | At3g51830 | 246300_at | ATG5 | contains similarity to phosphoinositide phosphatase SAC1 (Rattus norvegicus); putative transmembrane protein G5p (AtG5) | 2 | Lipid signaling | 1.48 | 4.66 | ||||||||||||||||||||||||||||
page created by Vincent Sauveplane | 05/19/06 |