| Co-Expression Analysis of: | CYP76C2 (At2g45570) | Institut de Biologie Moléculaire des Plantes |
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| ________________________ | _____________________________________________ | CYPedia Home | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hormones etc. 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | >2.99 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| greater than zero | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| less than zero | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Locus | r-value | Name | Description | ethylene, 3h, petiole (13) | mock, 30min, seedling (110) | IAA, 30min, seedling (110) | IAA, 1h, seedling (110) | IAA, 3h, seedling (110) | zeatin, 30min, seedling (110) | zeatin, 1h, seedling (110) | zeatin, 3h, seedling (110) | GA3, 30min, seedling (110) | GA3, 1h, seedling (110) | GA3, 3h, seedling (110) | ABA, 30min, seedling (110) | ABA, 1h, seedling (110) | ABA, 3h, seedling (110) | MJ, 30min, seedling (110) | MJ, 1h, seedling (110) | MJ, 3h, seedling (110) | ACC, 30min, seedling (110) | ACC, 1h, seedling (110) | ACC, 3h, seedling (110) | BL, 30min, seedling (110) | BL, 1h, seedling (110) | BL, 3h, seedling (110) | ABA, 3 uM, imbided seed (116) | ABA, 30 uM, imbided seed (116) | GA, 3h, imbibed seed (119) | GA, 6h, imbibed seed (119) | GA, 9h, imbibed seed (119) | GA, 3h, imbibed seed (134) | GA, 6h, imbibed seed (134) | GA, 9h, imbibed seed (134) | GA, 30min, whole plant (99) | GA, 60min, whole plant (99) | GA, 3h, whole plant (99) | IAA, 0.1uM, 1h, seedling (144) | IAA, 0.1uM, 3h, seedling (144) | IAA, 1uM, 1h, seedling (144) | IAA, 1uM, 3h, seedling (144) | ppi, 3h, seedling (113) | ppi, 12h, seedling (113) | uni, 3h, seedling (113) | uni, 12h, seedling (113) | brz220, 3h, seedling (113) | brz220, 12h, seedling (113) | brz91, 3h, seedling (113) | brz91, 12h, seedling (113) | pac, 3h, seedling (113) | pac, 12h, seedling (113) | px, 3h, seedling (113) | px, 12h, seedling (113) | pno8, 3h, seedling (113) | pno8, 12h, seedling (113) | ibup, 3h, seedling (113) | B9, 3h, seedling (113) | AgNO3, 3h, seedling (113) | AVG, 3h, seedling (113) | Sal, 3h, seedling (113) | MG132, 3h, seedling (113) | 246T, 3h, seedling (113) | PCIB, 3h, seedling (113) | TIBA, 3h, seedling (113) | NPA, 3h, seedling (113) | CHX, 3h, seedling (113) | Colm, 3h, seedling (113) | ColPNO8, 3h, seedling (113) | ColBrz, 3h, seedling (113) | glucose, 8h, seedling (14) | sucrose, 8h, seedling (15) | deoxyglucose, 8h_seedling (14) | methylglucose, 8h, seedling (14) | K depleted, whole rosette (97) | K depleted, root (97) | Sulfate depleted, 2h, root (112) | Sulfate depleted, 4h, root (112) | Sulfate depleted, 8h, root (112) | Sulfate depleted, 12h, root (112) | Sulfate depleted, 24h, root (112) | mannitol, 8h, seedling (14) | CO2, 1000ppm, guard cell enriched (11) | CO2, 1000ppm, mature leaf (11) | CO2, high light, whole rosette (95) | CO2, medium light, whole rosette (95) | CO2, low light, whole rosette (95) | CO2, 2h, juvenile leaf (151) | CO2, 4h, juvenile leaf (151) | CO2, 6h, juvenile leaf (151) | CO2, 12h, juvenile leaf (151) | CO2, 24h, juvenile leaf (151) | CO2, 48h, juvenile leaf (151) | dark, 45min, seedling (109) | dark, 4h, seedling (109) | far red, 45min, seedling (109) | far red, 4h, seedling (109) | red pulse1, seedling (109) | red pulse2, seedling (109) | red, 45min, seedling (109) | red, 4h, seedling (109) | blue, 45min, seedling (109) | blue, 4h, seedling (109) | UV-A pulse1, seedling (109) | UV-A pulse2, seedling (109) | UV-AB pulse1, seedling (109) | UV-AB pulse2, seedling (109) | UV-A, 18h, mature leaf (72) | UV-B, 18h, mature leaf (72) | 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 |
| At2g45570 | 1.000 | CYP76C2 | cytochrome P450 family protein | -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 | 3.5 | -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 | -0.1 | -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 | -0.1 | -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 | 2.8 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 3.6 | At2g45570 | 267559_at | CYP76C2 | cytochrome P450 family protein | 1 | cytochrome P450 family | 0.00 | 3.76 | |||||||
| At1g09500 | 0.771 | similar to Eucalyptus gunnii alcohol dehydrogenase of unknown physiological function, NOT a cinnamyl-alcohol dehydrogenase | -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 | 2.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 1.1 | -0.8 | 0 | -0.1 | -0.8 | 0 | -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 | -0.1 | -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 | 3.4 | -0.1 | 0.3 | -0.1 | 0.9 | 0.9 | 3.6 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 1.6 | -0.1 | -1.1 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 4.5 | At1g09500 | 264514_at | similar to Eucalyptus gunnii alcohol dehydrogenase of unknown physiological function, NOT a cinnamyl-alcohol dehydrogenase | 2 | lignin biosynthesis | Phenylpropanoid pathway | 1.27 | 5.68 | ||||||||
| At2g13810 | 0.724 | aminotransferase class I and II family protein, low similarity to Aromatic Aminotransferase from Pyrococcus horikoshii | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.9 | 0.6 | 0 | 0 | 0 | 0 | 0 | 0 | -1 | 0 | 0 | 0 | 0 | 0 | 0 | 0.5 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2.5 | At2g13810 | 265658_at | aminotransferase class I and II family protein, low similarity to Aromatic Aminotransferase from Pyrococcus horikoshii | 2 | Carbon fixation | Glutamate metabolism | Alanine and aspartate metabolism | Cysteine metabolism | Arginine and proline metabolism | Tyrosine metabolism | Phenylalanine, tyrosine and tryptophan biosynthesis | Alkaloid biosynthesis I | Novobiocin biosynthesis | Phenylalanine metabolism | 0.00 | 3.64 | |||||||||
| At3g22600 | 0.676 | protease inhibitor/seed storage/lipid transfer protein (LTP) family protein | -2 | -0.1 | 0 | 0.2 | 0.2 | -0.2 | 0 | 0.2 | -0.1 | -0.2 | -0.3 | 0 | 0.5 | 1.4 | -0.3 | -0.1 | -0.6 | -0.1 | -0.1 | -0.1 | -0.2 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.2 | -0.1 | -0.1 | 0.2 | -0.4 | -0.3 | -0.7 | 0 | 0.2 | 0.4 | 0.1 | -0.2 | 0.1 | -0.3 | 0 | 0 | -0.1 | -0.2 | -0.1 | -0.2 | 0 | 0.2 | 0.3 | 0 | 0 | 0.3 | -0.1 | 0.9 | 0.1 | 0.9 | -0.2 | 0.7 | 0.3 | 1.1 | -0.5 | -0.4 | -0.3 | -0.5 | -0.1 | -0.7 | 0.6 | -0.8 | -0.9 | 3 | -0.1 | 0 | 0.3 | 0.3 | -0.1 | 0.1 | -0.7 | -1.2 | -1.4 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.1 | -0.1 | -0.1 | 0 | -0.4 | -0.1 | 0 | 0 | -0.2 | 0 | 0 | 0.1 | 0 | 0 | -0.1 | 0.1 | 0.3 | 1.6 | 3.4 | At3g22600 | 256933_at | protease inhibitor/seed storage/lipid transfer protein (LTP) family protein | 2 | Miscellaneous acyl lipid metabolism | 1.76 | 5.47 | |||||||||
| At4g34230 | 0.658 | CAD5 | Encodes a catalytically active cinnamyl alcohol dehydrogenase which uses p-coumaryl aldehyde as a preferred substrate. It can also use sinapyl, caffeyl, coniferyl and d-hydroxyconiferyl aldehydes as substrates. | -0.3 | 0 | -0.2 | 0 | 0.1 | 0 | 0.1 | -0.2 | 0 | 0.1 | 0.1 | 0.2 | 0.9 | 2.1 | -0.1 | 0.3 | 0.4 | 0 | 0 | 0.1 | 0.1 | 0.1 | -0.4 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0 | -0.3 | 0 | 0 | -0.2 | -0.1 | -0.1 | -0.1 | -0.3 | -0.2 | 0 | -0.2 | 0 | -0.1 | 0 | -0.2 | 0 | -0.1 | 0.1 | 0 | 0.1 | -0.1 | 0 | -0.2 | -0.1 | 0.9 | -0.2 | 0 | -0.2 | 0.1 | 0.1 | -0.2 | -0.2 | -1.9 | 0 | 0.1 | 0 | 0.1 | 0.3 | 0.4 | 0 | 1.7 | 0.5 | 0 | 0.1 | 0 | -0.1 | 0 | 0 | -0.4 | -0.9 | 0 | 0.1 | -0.5 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0 | -0.1 | 0 | -0.2 | 0 | -0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0.4 | 1 | At4g34230 | 253277_at | CAD5 | Encodes a catalytically active cinnamyl alcohol dehydrogenase which uses p-coumaryl aldehyde as a preferred substrate. It can also use sinapyl, caffeyl, coniferyl and d-hydroxyconiferyl aldehydes as substrates. | 10 | cinnamyl-alcohol dehydrogenase activity | lignin biosynthesis | biogenesis of cell wall | lignin biosynthesis | Stilbene, coumarine and lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 0.92 | 4.11 | ||
| At3g49210 | 0.645 | expressed protein | 0 | 0 | 0 | 0.1 | 0.2 | 0 | -0.2 | 0 | 0.1 | 0.1 | 0.1 | 0 | -0.2 | 0.9 | -0.5 | -0.4 | -0.6 | 0.1 | 0 | 0.2 | 0 | 0.2 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.4 | 0.6 | 0.1 | -0.2 | -0.1 | 0.1 | -0.2 | -0.4 | 0 | -0.2 | 0 | -0.4 | -0.1 | -0.2 | 0.1 | -0.1 | 0.1 | 0 | 0.2 | -0.3 | 0.5 | -0.5 | -0.2 | 0.4 | -0.2 | 0.4 | -0.3 | -0.6 | 0 | -0.4 | -0.1 | 0.2 | -0.1 | 0.3 | 0.1 | 0 | 0.2 | 0 | 0.2 | 1.9 | 0 | 0 | 0.1 | -0.1 | 0 | -0.1 | 0 | 0 | -1.7 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0.2 | 0 | -0.1 | 0 | -0.1 | 0 | 0 | 0 | -0.1 | 0.1 | 0 | 0 | 1.5 | At3g49210 | 252303_at | expressed protein | 2 | Fatty acid elongation and wax and cutin metabolism | 0.98 | 3.76 | |||||||||
| At5g20830 | 0.642 | SUS1 | sucrose synthase / sucrose-UDP glucosyltransferase | -0.2 | 0 | 0 | -0.1 | 0.2 | 0 | 0 | 0 | 0.1 | 0 | 0 | 0.1 | 0.4 | 3.4 | -0.1 | -0.1 | -0.2 | 0.1 | 0 | 0.2 | 0.1 | 0.1 | 0 | 0.4 | 0.2 | -0.4 | 0 | -0.2 | -0.4 | 0 | -0.2 | -0.1 | 0.4 | 0.1 | 0.5 | 0.5 | -0.2 | -0.4 | 0 | 0 | -0.3 | 0 | 0.1 | -0.5 | 0.1 | 0.3 | 0.2 | -0.3 | -0.6 | 0.1 | 0 | -0.3 | 0.1 | -0.1 | 0.3 | -0.5 | 0 | -0.6 | -0.1 | -0.1 | -0.1 | 0 | -0.5 | -0.7 | 0.4 | -0.7 | -0.5 | 1.8 | 0.2 | 0 | 0.7 | 0 | 0 | 0.2 | 0.2 | 0.3 | 0 | 0 | -0.5 | 0 | 0.2 | 0.4 | -0.4 | 0 | 0.1 | 0 | 0 | 0.3 | -0.1 | -0.2 | -0.9 | 0 | -0.2 | -0.2 | -0.9 | -0.2 | -0.9 | -0.2 | 0 | -0.2 | 0 | -0.2 | 0.2 | -0.2 | 1.5 | At5g20830 | 245998_at | SUS1 | sucrose synthase / sucrose-UDP glucosyltransferase | 10 | response to cold | response to flooding | C-compound, carbohydrate anabolism | glycolysis and gluconeogenesis | sucrose biosynthesis | sucrose degradation III | Starch and sucrose metabolism | Cell Wall Carbohydrate Metabolism | sucrose metabolism | 1.21 | 4.37 | |||
| At3g01420 | 0.641 | ALPHA-DOX1 | Encodes an alpha-dioxygenase involved in protection against oxidative stress and cell death. | -0.1 | -0.1 | -0.2 | 0.5 | 0.2 | 0 | 0.5 | 0 | 0 | 0.3 | -0.4 | -0.4 | 0.5 | 2.7 | -0.5 | 0.3 | 0 | -0.1 | 0 | -0.2 | -0.7 | 0.4 | -0.3 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.1 | -0.6 | 0.3 | 0.1 | 0.3 | -0.3 | -0.5 | 0.6 | -0.4 | 0.3 | -0.4 | 0.4 | -0.2 | 0.3 | 0 | 0.5 | -0.1 | 0.3 | -0.4 | 0.2 | 0 | -0.3 | -0.9 | 0 | 1.3 | -0.9 | 0.5 | 0.4 | 0 | -0.3 | -1 | -1 | -2 | -0.7 | -0.7 | 1.8 | 0 | -0.2 | 1.6 | 0.3 | -0.1 | 0.2 | 0 | 0.1 | 0.1 | -0.1 | -1.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | 0.1 | 0 | 0 | 0 | -0.1 | -0.2 | 0 | 0 | 0.3 | 0.2 | 0.2 | -0.1 | 0.2 | -0.1 | 2.5 | At3g01420 | 258957_at | ALPHA-DOX1 | Encodes an alpha-dioxygenase involved in protection against oxidative stress and cell death. | 10 | lipoxygenase activity | fatty acid alpha-oxidation | cell death | jasmonic acid biosynthesis | lipoxygenase pathway | Lipid signaling | 1.57 | 4.78 | |||||
| At2g29090 | 0.637 | CYP707A2 | cytochrome P450 family protein, similar to taxane 13-alpha-hydroxylase (Taxus cuspidata). | 0.7 | -0.2 | -0.3 | -0.4 | 0.4 | -0.5 | -0.6 | -0.8 | -0.3 | 0 | -0.8 | 0 | 1.6 | 3 | -1 | -0.6 | -0.8 | -1 | 0.1 | -0.1 | -0.2 | -0.6 | -0.8 | 0.8 | 0.9 | 0.8 | 0.2 | 0.3 | 0.8 | 0.2 | 0.3 | -0.1 | -0.6 | -0.6 | 0.3 | -0.1 | -0.2 | 0 | 0.6 | -0.3 | -0.1 | 0 | 0.6 | -0.2 | 0.1 | -0.3 | -0.2 | -0.1 | -0.2 | 0.2 | 0.6 | -0.3 | 0.5 | -0.2 | -0.2 | -0.2 | -0.2 | 0.6 | 0.2 | -0.2 | -0.2 | 0.3 | 0.8 | -0.2 | -0.2 | -0.2 | 0.7 | -0.4 | 0.8 | 0.3 | 2.6 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.2 | -1.4 | -0.7 | 0 | -1.1 | -0.2 | -0.4 | -0.5 | 0.3 | -0.2 | 0 | 0.1 | -0.2 | -0.2 | -0.2 | 1.2 | -0.2 | -0.2 | -0.2 | -0.2 | -0.2 | 0.1 | 0.3 | -0.2 | -0.2 | -0.2 | -0.2 | 1.8 | At2g29090 | 266778_at | CYP707A2 | cytochrome P450 family protein, similar to taxane 13-alpha-hydroxylase (Taxus cuspidata). | 10 | degradation of abscisic acid | cytochrome P450 family, 8’-hydroxylase for ABA, degradation of abscisic acid | 1.76 | 4.47 | ||||||
| At5g66760 | 0.637 | SDH1-1 | One of two genes in Arabidopsis that encode a flavoprotein subunit of the mitochondrial succinate dehydrogenase complex. | 0 | 0 | -0.2 | 0 | 0.1 | 0 | -0.2 | 0 | 0 | 0 | 0.1 | -0.2 | 0 | 1.3 | -0.2 | 0 | 0.1 | -0.3 | -0.2 | 0.1 | -0.1 | -0.2 | 0 | 0 | 0 | -0.1 | 0 | 0.1 | -0.1 | 0 | 0.1 | -0.3 | 0 | 0 | 0.1 | 0 | 0 | -0.3 | 0.2 | 0 | 0.3 | -0.1 | 0.1 | 0 | 0 | -0.2 | -0.1 | -0.1 | -0.2 | 0 | 0 | -0.1 | 0.2 | -0.1 | 0 | -0.1 | 0 | 0.2 | 0.1 | 0 | 0 | 0.3 | -0.6 | -0.1 | -0.1 | -0.1 | 0.3 | 0.8 | 0.1 | 0.1 | 0.1 | -0.3 | 0.1 | -0.1 | 0 | 0 | 0.1 | 0 | -0.5 | -0.4 | -0.2 | -0.3 | 0 | 0 | 0 | 0.1 | 0.1 | 0.2 | 0 | 0 | -0.6 | 0 | 0.3 | 0 | -0.5 | -0.1 | -0.5 | 0.1 | 0.1 | 0.1 | -0.6 | 0 | 0.5 | 0.1 | 2 | At5g66760 | 247060_at | SDH1-1 | One of two genes in Arabidopsis that encode a flavoprotein subunit of the mitochondrial succinate dehydrogenase complex. | 4 | succinate dehydrogenase activity | mitochondrial electron transport, succinate to ubiquinone | C-compound and carbohydrate metabolism | tricarboxylic-acid pathway (citrate cycle, Krebs cycle, TCA cycle) | aerobic respiration -- electron donors reaction list | TCA cycle -- aerobic respiration | Citrate cycle (TCA cycle) | Oxidative phosphorylation | Intermediary Carbon Metabolism | Gluconeogenesis from lipids in seeds | 0.80 | 2.66 | |||
| At5g10730 | 0.636 | expressed protein | 0 | 0 | -0.1 | -0.1 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0.2 | 0.1 | 1.6 | 0 | 0 | 0.2 | 0.2 | 0.1 | 0 | 0.1 | 0.2 | -0.1 | 0.3 | 0.6 | 0.1 | 0 | -0.3 | 0.1 | 0 | -0.3 | -0.1 | -0.2 | 0 | 0 | 0.1 | 0 | -0.2 | 0 | -0.1 | 0 | -0.1 | 0.1 | -0.1 | 0 | -0.1 | 0 | -0.1 | 0.1 | 0 | 0 | 0 | 0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | -0.2 | -0.3 | 0 | 0 | -0.1 | 0.1 | -0.3 | 0 | 0.4 | 0 | 0 | 0 | 0 | 0.3 | 0.1 | -0.4 | -0.5 | 0 | -0.2 | 0.1 | -0.2 | 0 | 0 | -0.1 | 0 | 0 | 0.1 | -0.2 | -0.1 | -0.1 | 0.2 | -0.2 | -0.3 | -0.2 | -0.1 | 0 | 0.1 | 0 | -0.3 | -0.1 | 0.5 | -0.2 | 0.7 | At5g10730 | 246017_at | expressed protein | 1 | colanic acid building blocks biosynthesis | dTDP-rhamnose biosynthesis | galactose degradation I | UDP-glucose conversion | lactose degradation IV | 0.65 | 2.20 | |||||||||
| At1g74020 | 0.635 | SS2 | strictosidine synthase family protein / AtSS-2 strictosidine synthase (SS) | 0 | 0 | -0.2 | 0 | -0.2 | -0.1 | 0.2 | 0 | -0.2 | -0.1 | -0.3 | -0.3 | 0 | 1.5 | -0.5 | 0 | 0.3 | -0.4 | -0.3 | -0.3 | -0.3 | -0.5 | -0.8 | -0.1 | -0.1 | -0.2 | 0.4 | 1.4 | -0.2 | 0.4 | 1.4 | 0 | -0.1 | -0.3 | 0 | 0.2 | 0 | -0.1 | 0.1 | 0.3 | 0 | 0.4 | 0 | 0.1 | 0 | 0 | 0.1 | 0.2 | 0 | 0.1 | -0.3 | 0 | 0.1 | 0 | 0.5 | 0.1 | 0.3 | -0.4 | 0 | 0 | 0 | -0.1 | -1.1 | -0.5 | -0.8 | -0.4 | -0.1 | -0.1 | -0.1 | -0.1 | 2.3 | 0.4 | 0 | 0 | -0.1 | -0.1 | 0 | 0 | -0.3 | -0.1 | -0.6 | -0.3 | 0 | 0 | -0.1 | 0 | 0 | -0.2 | 0 | 0 | 0 | -0.2 | 0 | -0.1 | -0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | 1.4 | At1g74020 | 260391_at | SS2 | strictosidine synthase family protein / AtSS-2 strictosidine synthase (SS) | 2 | Terpenoid biosynthesis | Indole and ipecac alkaloid biosynthesis | 1.05 | 3.47 | |||||||
| At1g80160 | 0.630 | lactoylglutathione lyase family protein / glyoxalase I family protein | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | -0.1 | 0 | 3.7 | 0 | 0 | 0.3 | 0 | 0.3 | -0.1 | 0 | 0 | 0 | 0.6 | 0.5 | -0.3 | -0.5 | -1 | -0.3 | -0.5 | -1 | 0 | 0.4 | 0 | -0.4 | -0.2 | -0.3 | -0.3 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0.6 | -0.1 | -2.1 | -1.8 | 1.4 | 1.7 | 2.2 | 0.3 | 0 | -0.1 | 0 | 0 | 0 | 2.2 | -2.4 | -1.4 | 0 | 0 | 0 | 0 | 0.3 | 0 | 0 | 0 | 0 | 0.2 | 1 | 0 | -0.2 | 0 | 0.5 | 0 | 0.1 | -0.2 | -0.3 | -0.1 | 0 | -0.5 | -0.9 | 0 | 2.2 | At1g80160 | 262047_at | lactoylglutathione lyase family protein / glyoxalase I family protein | 2 | threonine degradation | methylglyoxal degradation | 2.41 | 6.14 | |||||||||
| At4g03320 | 0.625 | similar to P. sativum Tic20 chloroplast protein import component | -0.1 | -0.1 | 0.1 | 0.4 | 0.2 | -0.1 | -0.8 | -0.1 | -0.1 | 0.4 | -0.4 | -0.1 | -0.8 | 1.5 | -0.1 | -0.8 | -1.3 | -0.1 | -0.8 | -0.4 | -0.1 | -0.8 | -0.8 | 0 | 0 | 0.1 | 0 | -0.1 | 0.1 | 0 | -0.1 | -2.1 | -0.8 | -2.1 | -0.1 | 0.3 | -0.2 | 0 | 0 | 0.9 | 0 | 0.3 | 0 | 0.4 | -0.2 | 0 | 0.1 | 0.5 | -0.4 | 0.6 | 0.2 | 0.8 | -0.1 | 0 | 1.3 | -0.3 | 0.7 | 1 | 0.4 | -1.8 | 1.2 | -0.5 | -1.8 | -0.5 | 0.2 | -0.1 | 0.2 | 0 | 0.9 | 0.7 | 3.3 | 0.3 | 0 | -0.1 | 0 | 0.2 | 0 | 1.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | 0 | -0.5 | -0.1 | -0.2 | -0.2 | -0.3 | 0 | -0.4 | 0 | -0.1 | -0.1 | 0.1 | 1.1 | -0.1 | 4 | At4g03320 | 255430_at | similar to P. sativum Tic20 chloroplast protein import component | 4 | protein targeting, sorting and translocation | transport routes | chloroplast transport | biogenesis of chloroplast | Chloroplastic protein import via envelope membrane | Tic apparatus | 2.11 | 6.15 | ||||||||
| At1g76470 | 0.616 | cinnamoyl-CoA reductase family | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.3 | 0 | 0 | -0.3 | -0.7 | -0.4 | -0.7 | 0 | 0.3 | 0 | -0.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0.6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.8 | 0 | 0 | 0.2 | 0 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.2 | At1g76470 | 259975_at | cinnamoyl-CoA reductase family | 2 | lignin biosynthesis | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 0.59 | 2.56 | |||||||
| At5g39090 | 0.616 | transferase family protein, similar to anthocyanin 5-aromatic acyltransferase from Gentiana triflora, malonyl CoA:anthocyanin 5-O-glucoside-6'''-O-malonyltransferase from Perilla frutescens and Salvia splendens | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 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 | 0.9 | 0 | 0.9 | 0 | 0.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.9 | 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 | 1.8 | At5g39090 | 249489_at | transferase family protein, similar to anthocyanin 5-aromatic acyltransferase from Gentiana triflora, malonyl CoA:anthocyanin 5-O-glucoside-6'''-O-malonyltransferase from Perilla frutescens and Salvia splendens | 1 | protein modification | Phenylpropanoid Metabolism | Flavonoid and anthocyanin metabolism | acyltransferase, BAHD family, group B, AT-like | 0.14 | 2.29 | |||||||
| At3g23920 | 0.612 | beta-amylase, putative / 1,4-alpha-D-glucan maltohydrolase, putative | -0.3 | 0 | 0 | 0 | -0.2 | 0 | -0.1 | -0.4 | 0 | 0 | -0.4 | 0.4 | 1.3 | 3.2 | -0.4 | 0 | -0.1 | -0.3 | -0.2 | -0.4 | -0.4 | -0.5 | -0.7 | 0 | 0.3 | 0.2 | 0.3 | 0.3 | 0.2 | 0.3 | 0.3 | -0.1 | 0.2 | -0.2 | 0 | 0 | -0.2 | -0.3 | 0 | 0.1 | 0 | 0.5 | 0 | 0.2 | 0.2 | 0.4 | 0 | 0.4 | 0.1 | 0.2 | 0.1 | 0.2 | 0.1 | 0 | 0.3 | -0.1 | 0 | 0 | 0 | -0.4 | 0.3 | -0.1 | -0.9 | 0.2 | 0 | 0.4 | -0.4 | 0.1 | 0.3 | 0.2 | 1.4 | 0.2 | 0 | 0.1 | -0.1 | 0 | 0.1 | 0 | -1.5 | -1.3 | -0.4 | 0 | -0.4 | 0 | -0.1 | -0.2 | -0.1 | 0 | 0 | -0.7 | -0.4 | -0.2 | 0.3 | -0.2 | -0.4 | -0.3 | 0 | 0 | 0.1 | 0.3 | -0.4 | 0.1 | 0 | 0 | 0.8 | At3g23920 | 256861_at | beta-amylase, putative / 1,4-alpha-D-glucan maltohydrolase, putative | 4 | C-compound and carbohydrate metabolism | metabolism of energy reserves (e.g. glycogen, trehalose) | starch degradation | Cell Wall Carbohydrate Metabolism | starch metabolism | 0.94 | 4.76 | |||||||
| At2g04350 | 0.602 | long-chain-fatty-acid--CoA ligase family protein / long-chain acyl-CoA synthetase family protein (LACS8) | -0.1 | 0 | 0 | -0.1 | 0 | -0.6 | 0.1 | -0.2 | -0.2 | 0.1 | -0.3 | 0.1 | 1.2 | 3.2 | -0.3 | 0.2 | 0.1 | -0.2 | -0.1 | 0 | -0.1 | 0.1 | -0.5 | 0.4 | 0.9 | -0.4 | 0.1 | 0 | -0.4 | 0.1 | 0 | -0.2 | -0.1 | -0.3 | 0 | 0.1 | 0.1 | 0 | 0.1 | 0 | 0.1 | 0 | 0.1 | -0.1 | 0 | 0 | 0 | 0 | 0.4 | 0.1 | 0.1 | 0 | 0.2 | 0 | -0.1 | 0 | 0.1 | 0.1 | 0.1 | 0 | 0.2 | 0.3 | 0 | -0.1 | -0.3 | 0.1 | -0.5 | 0.2 | -0.3 | -0.3 | 0.2 | 0 | 0.1 | 0.1 | 0.2 | 0.4 | 0 | -0.3 | -1.5 | -1.4 | -0.2 | 0.1 | -0.5 | 0 | 0 | 0 | -0.3 | 0 | 0 | -0.3 | -0.7 | -0.1 | 0.2 | -0.1 | -0.6 | 0 | -0.3 | 0 | 0 | 0.2 | -0.4 | -0.1 | 0.3 | 0.5 | 1.5 | At2g04350 | 263811_at | long-chain-fatty-acid--CoA ligase family protein / long-chain acyl-CoA synthetase family protein (LACS8) | 10 | fatty acid oxidation pathway | octane oxidation | Fatty acid metabolism | Gluconeogenesis from lipids in seeds | Miscellaneous acyl lipid metabolism | Acyl activating enzymes , CoA ligases, clade I, long-chain acyl-CoA synthetases | 1.05 | 4.79 | |||||
| At2g34850 | 0.602 | NAD-dependent epimerase/dehydratase family protein, similar to UDP-galactose 4-epimerase from Cyamopsis tetragonoloba and Lactococcus lactis | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | At2g34850 | 267429_at | NAD-dependent epimerase/dehydratase family protein, similar to UDP-galactose 4-epimerase from Cyamopsis tetragonoloba and Lactococcus lactis | 2 | colanic acid building blocks biosynthesis | dTDP-rhamnose biosynthesis | galactose degradation I | UDP-glucose conversion | lactose degradation IV | Galactose metabolism | Nucleotide sugars metabolism | 0.00 | 2.06 | ||||||||
| At3g46660 | 0.602 | UDP-glucoronosyl/UDP-glucosyl transferase family protein | -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 | 2.3 | -0.1 | -0.1 | 1.6 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.2 | -0.4 | -0.4 | -1.4 | -0.4 | -0.4 | -1.4 | -0.1 | -0.1 | -0.1 | -0.1 | 1.4 | -0.1 | -0.5 | -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 | 4.1 | -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 | 1.9 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 2.8 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 3.4 | At3g46660 | 252487_at | UDP-glucoronosyl/UDP-glucosyl transferase family protein | 1 | C-compound and carbohydrate metabolism | Glycosyl transferase, Family 1 | 2.04 | 5.57 | ||||||||
| At5g04380 | 0.602 | S-adenosyl-L-methionine:carboxyl methyltransferase family protein, similar to SAM:salicylic acid carboxyl methyltransferase (SAMT) (Clarkia breweri) and to SAM:benzoic acid carboxyl methyltransferase (Antirrhinum majus) | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2.4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 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 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | At5g04380 | 245703_at | S-adenosyl-L-methionine:carboxyl methyltransferase family protein, similar to SAM:salicylic acid carboxyl methyltransferase (SAMT) (Clarkia breweri) and to SAM:benzoic acid carboxyl methyltransferase (Antirrhinum majus) | 2 | secondary metabolism | Methyltransferase, SABATH family | 0.00 | 2.58 | ||||||||
| At3g09640 | 0.598 | APX2 | L-ascorbate peroxidase | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 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 | At3g09640 | 258695_at | APX2 | L-ascorbate peroxidase | 8 | L-ascorbate peroxidase activity | ascorbate glutathione cycle | Ascorbate and aldarate metabolism | Cell Wall Carbohydrate Metabolism | ascorbic acid biosynthesis | 0.00 | 3.49 | ||||
| At4g09820 | 0.597 | TT8 | basic helix-loop-helix (bHLH) family protein, Affects dihydroflavonol 4-reductase gene expression. TRANSPARENT TESTA8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 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 | At4g09820 | 255056_at | TT8 | basic helix-loop-helix (bHLH) family protein, Affects dihydroflavonol 4-reductase gene expression. TRANSPARENT TESTA8 | 8 | flavonoid biosynthesis | transcription | RNA synthesis | mRNA synthesis | transcriptional control | Phenylpropanoid Metabolism | Flavonoid and anthocyanin metabolism | 0.00 | 3.25 | |||||
| At4g37990 | 0.593 | ELI3-2 | Encodes an aromatic alcohol:NADP+ oxidoreductase whose mRNA levels are increased in response to treatment with a variety of phytopathogenic bacteria. Though similar to mannitol dehydrogenases, this enzyme does not have mannitol dehydrogenase activity. | -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 | 0.6 | -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 | -0.4 | 0.7 | -0.4 | -0.2 | 0.3 | -0.2 | -0.5 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 1.8 | -0.1 | 1.7 | 1.6 | 1.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 2.2 | -1.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.1 | -0.3 | -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 | 4.3 | At4g37990 | 252984_at | ELI3-2 | Encodes an aromatic alcohol:NADP+ oxidoreductase whose mRNA levels are increased in response to treatment with a variety of phytopathogenic bacteria. Though similar to mannitol dehydrogenases, this enzyme does not have mannitol dehydrogenase activity. | 10 | aryl-alcohol dehydrogenase activity | mannitol dehydrogenase activity | response to bacteria | hypersensitive response | biogenesis of cell wall | sorbitol fermentation | mixed acid fermentation | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 1.41 | 5.48 | |||
| At3g19270 | 0.591 | CYP707A4 | cytochrome P450 family protein | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.9 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 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 | At3g19270 | 257035_at | CYP707A4 | cytochrome P450 family protein | 10 | degradation of abscisic acid | cytochrome P450 family, 8’-hydroxylase for ABA, degradation of abscisic acid | 0.00 | 2.38 | ||||||
| At2g37870 | 0.587 | protease inhibitor/seed storage/lipid transfer protein (LTP) family protein | -0.3 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | -0.2 | 0 | -0.3 | 0 | 0.3 | 4.5 | 0 | 0 | -0.3 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0.2 | -0.2 | 0 | 0 | -0.2 | 0 | 0 | -0.2 | 0 | 0.2 | -0.8 | 0.1 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | -0.2 | 0 | -0.2 | -0.3 | 0 | 0.6 | 0.4 | 0 | -0.3 | 0.1 | 0 | 0 | -0.1 | 0.1 | 0 | 0.2 | 0.7 | 0 | 0 | 0 | 0 | 0 | 0 | -0.6 | 2 | -0.6 | -0.6 | 1.7 | 0.4 | 0.3 | 0.1 | 0.2 | 0 | 0.5 | -0.6 | -1.2 | -0.6 | -1.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | -0.1 | -0.2 | -0.2 | 0 | -0.1 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.3 | 0.2 | 0 | At2g37870 | 266098_at | protease inhibitor/seed storage/lipid transfer protein (LTP) family protein | 2 | Miscellaneous acyl lipid metabolism | 1.12 | 5.80 | |||||||||
| At3g48520 | 0.582 | CYP94B3 | cytochrome P450 family protein, similar to P450-dependent fatty acid omega-hydroxylase (Vicia sativa) | -0.1 | -0.1 | 0.3 | 0 | 0.3 | 0 | 0.1 | -0.4 | -0.1 | -0.3 | -0.5 | 0.8 | 1.4 | 2.7 | 0.2 | 0.4 | 0 | -0.4 | 0 | -0.2 | -0.3 | 0.1 | -0.2 | -0.1 | -0.1 | 0 | -0.3 | 0 | 0 | -0.3 | 0 | 0.7 | 0 | -0.6 | 0.9 | 0.4 | 0.4 | 0.1 | -0.5 | 0.6 | -0.4 | 0.3 | 0 | 0 | -0.4 | 0.2 | 0 | 0.3 | 0 | 0.7 | -0.1 | 0.1 | -0.3 | -0.4 | -0.4 | -0.3 | -0.2 | -0.6 | -0.1 | -0.2 | 1.1 | -0.6 | 0.3 | -0.3 | -0.7 | -0.2 | -0.1 | -0.3 | -0.1 | -0.1 | 1.3 | 0.6 | 0 | 0.2 | -0.1 | -0.2 | 0 | -0.1 | -1.1 | -0.6 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.6 | 0.2 | -0.4 | 0.3 | -0.3 | -0.1 | -0.4 | -0.3 | -0.2 | 0.2 | 0.4 | 0 | -0.5 | 0.6 | -0.1 | 1.1 | At3g48520 | 252368_at | CYP94B3 | cytochrome P450 family protein, similar to P450-dependent fatty acid omega-hydroxylase (Vicia sativa) | 4 | lipid, fatty acid and isoprenoid metabolism | biogenesis of cell wall | cytochrome P450 family | 1.57 | 3.88 | ||||||
| At2g29470 | 0.574 | ATGSTU3 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | -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 | 0.6 | -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 | -0.1 | 0.9 | -0.1 | -0.6 | -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 | 1.5 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 2.7 | -0.1 | -0.1 | -0.1 | 3.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 2.4 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 1.7 | -0.1 | -2.4 | -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 | 1.8 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 4.8 | At2g29470 | 266270_at | ATGSTU3 | 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 | 1.88 | 7.38 | ||||||
| At1g48320 | 0.571 | thioesterase family protein, similar to ComAB (Bacillus licheniformis) | 1.6 | -0.2 | 0 | 0 | 0.3 | -0.4 | -0.4 | -0.1 | -0.2 | 0 | -0.1 | 0 | 0.1 | 1.6 | -0.4 | -0.5 | -0.9 | -0.4 | 0.2 | 0.4 | -0.1 | 0 | -0.4 | -0.1 | -0.6 | -0.6 | 0.3 | 0.5 | -0.6 | 0.3 | 0.5 | 0 | 0 | -0.3 | -0.2 | -0.3 | -0.2 | -0.5 | 0 | 0 | 0 | 0.3 | -0.1 | 0.2 | 0 | 0.1 | 0 | 0.1 | 0 | -0.1 | 0.2 | -0.1 | 0 | -0.1 | 0.4 | -0.3 | 0.5 | 0 | 0 | 0 | 0.4 | -0.2 | 1.6 | -0.1 | 0.5 | -0.1 | 0.4 | 0 | 0.4 | 0.3 | 1.9 | 0.4 | -0.1 | -0.2 | -0.3 | -0.1 | 0 | 0.4 | -0.6 | -0.8 | -0.8 | 0 | -0.3 | 0 | -0.1 | -0.4 | -0.1 | -0.2 | -0.1 | 0.1 | -0.2 | 0 | -0.1 | 0 | -0.3 | 0 | -0.4 | 0 | -0.2 | 0.1 | -0.3 | 0.5 | -0.1 | 0 | 1.4 | At1g48320 | 262237_at | thioesterase family protein, similar to ComAB (Bacillus licheniformis) | 2 | Gluconeogenesis from lipids in seeds | fatty acid beta oxidation complex | 1.20 | 2.88 | |||||||||
| At3g62590 | 0.567 | lipase class 3 family protein | 0 | 0 | -0.2 | -0.2 | 0 | 0 | 0.2 | 0 | -0.1 | 0 | 0 | 0 | 0.4 | 2.8 | -0.1 | -0.3 | -0.2 | 0 | 0 | -0.1 | 0 | 0.2 | 0 | -0.3 | 0.3 | -0.2 | 0.4 | 0.2 | -0.2 | 0.4 | 0.2 | -0.2 | 0 | 0.4 | 0.1 | 0.2 | 0 | -0.3 | 0 | -0.3 | -0.6 | -0.1 | -0.4 | -0.2 | 0 | 0 | -0.2 | 0 | -0.1 | -0.5 | -0.2 | 0 | -0.2 | -0.1 | 0 | 0 | 0 | -0.2 | -0.1 | 0.5 | 0.5 | 0 | -0.1 | -0.2 | 0.5 | 0 | 0 | 0 | 0.1 | 0 | 1.2 | 0 | -0.3 | 0.4 | 0.1 | 0.1 | 0 | 0 | -0.3 | -0.8 | -0.2 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | 0.2 | 0 | -0.1 | 0 | 0 | 0 | 0.1 | 0 | -0.3 | 0 | -0.1 | -0.4 | -0.1 | -0.1 | -0.1 | At3g62590 | 251191_at (m) | lipase class 3 family protein | 2 | triacylglycerol degradation | Miscellaneous acyl lipid metabolism | 0.86 | 3.70 | ||||||||
| At1g68620 | 0.558 | similar to PrMC3 (Pinus radiata) | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | 0.5 | 2.9 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.8 | -0.3 | -1.7 | 0.2 | -0.3 | -0.3 | -0.7 | 0 | 0 | -0.8 | -0.3 | -0.8 | -0.2 | -0.3 | 0.7 | 0 | 0.4 | 0.7 | 0.2 | 1.1 | 0.9 | 1.2 | -0.8 | 2.4 | -0.8 | 0.4 | -0.8 | 1.4 | 0.6 | 2.8 | -0.8 | 2.3 | -0.8 | 1.7 | -0.8 | -0.7 | -1.5 | 0.1 | 0 | 2.5 | 0.6 | 0 | 0.4 | 0.9 | 0.9 | 0 | 0.6 | -4.1 | -2.1 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.3 | -0.9 | 0 | -0.4 | 0.3 | -0.2 | -0.3 | -0.3 | -0.3 | -0.5 | 0.2 | 0.4 | -0.2 | 1 | 0.6 | 1.8 | 4.6 | At1g68620 | 262229_at | similar to PrMC3 (Pinus radiata) | 2 | carboxylesterase | 3.14 | 8.76 | |||||||||
| At2g36770 | 0.556 | UDP-glucoronosyl/UDP-glucosyl transferase family protein | -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 | 2.7 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.4 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.9 | -0.1 | 0.2 | -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 | 2.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.6 | -0.1 | 1.5 | -0.1 | 3.5 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0.4 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 1.4 | -1.1 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 2.6 | At2g36770 | 265199_s_at | UDP-glucoronosyl/UDP-glucosyl transferase family protein | 1 | Glycosyl transferase, Family 1 | 1.50 | 4.73 | |||||||||
| At5g53120 | 0.551 | SPDS3 | encodes a novel spermine synthase and is a paralog of previously characterized spermidine synthases, SPDS1 and SPDS2. SPDS3 forms heterodimers with SDPS2, which in turn forms heterodimers with SDPS1 in vivo. The gene does not complement speDelta3 deficien | -0.2 | 0 | 0 | 0 | -0.2 | -0.1 | 0.3 | -0.3 | -0.1 | 0.2 | -0.2 | -0.1 | 0.9 | 2.7 | -0.2 | -0.2 | -0.4 | -0.5 | -0.1 | -0.5 | -0.4 | 0 | 0 | 0 | 0 | 0.2 | 0.2 | 0.1 | 0.2 | 0.2 | 0.1 | 0 | 0 | 0.8 | 0 | 0 | -0.1 | -0.2 | 0.1 | 0 | 0 | -0.4 | 0.3 | 0.1 | 0.1 | -0.2 | -0.1 | -0.2 | 0.3 | 0.2 | 0 | 0 | 0.1 | 0.1 | -0.5 | 0.2 | 0.7 | -0.1 | 0.3 | 0.4 | 0.4 | 0.3 | -0.9 | 0.3 | 0 | 0.3 | -0.1 | 0.3 | 0 | -0.2 | 0.3 | -0.4 | 0 | 0 | -0.2 | 0.1 | 0.1 | -0.1 | -0.5 | -0.2 | -0.3 | -0.3 | -1.2 | 0 | 0 | -0.1 | 0 | -0.2 | 0 | -0.1 | -1 | -0.4 | 0.1 | 0 | -0.8 | -0.1 | -0.3 | 0 | 0 | 0.5 | -0.6 | 0.1 | 0 | 0.3 | 1 | At5g53120 | 248250_at (m) | SPDS3 | encodes a novel spermine synthase and is a paralog of previously characterized spermidine synthases, SPDS1 and SPDS2. SPDS3 forms heterodimers with SDPS2, which in turn forms heterodimers with SDPS1 in vivo. The gene does not complement speDelta3 deficien | 9 | spermidine synthase activity | polyamine biosynthesis | spermine biosynthesis I | polyamine biosynthesis II | spermine biosynthesis II | polyamine biosynthesis III | polyamine biosynthesis I | Arginine and proline metabolism | Urea cycle and metabolism of amino groups | beta-Alanine metabolism | 1.15 | 4.05 | |||||
| At4g31870 | 0.541 | ATGPX7 | Encodes glutathione peroxidase. | -0.6 | -0.2 | -0.3 | 0 | -0.1 | 0 | -0.2 | 0.3 | -0.1 | 0 | 0.6 | -0.5 | 0 | 0.3 | 0 | 0.2 | 0.8 | 0.1 | 0 | 0.1 | 0.4 | 0 | 0.3 | 0.2 | 0 | -0.6 | -0.2 | -0.2 | -0.6 | -0.2 | -0.2 | -0.3 | -0.2 | 0 | 0.1 | 0.5 | -0.3 | -0.5 | 0.5 | -0.6 | -0.4 | -0.7 | 0 | -0.6 | 0.7 | -0.3 | 0 | -0.6 | 0.4 | -0.6 | 0.4 | -0.1 | 0.5 | 0.2 | 0.3 | 0.2 | 0.3 | 0.6 | 0.3 | 1 | 0.7 | 0.2 | 1.3 | -0.4 | 0.4 | -0.3 | -0.4 | 0 | -0.1 | -0.3 | 1.5 | 0 | -0.2 | 0.1 | 0.3 | -0.4 | 0.1 | 0 | -0.3 | -0.3 | -0.9 | 0.3 | 0 | -0.5 | -0.1 | -0.1 | -0.2 | -0.3 | -0.3 | 0 | -0.5 | 0 | 1 | 0 | -0.8 | -0.3 | -0.7 | 0 | -0.1 | -0.1 | -1 | -0.3 | -0.2 | 0.5 | 3.5 | At4g31870 | 253496_at | ATGPX7 | Encodes glutathione peroxidase. | 6 | detoxification | Glutathione metabolism | Biosynthesis of Amino Acids and Derivatives | Glutathione metabolism | 1.52 | 4.68 | |||||
| At3g12500 | 0.535 | ATHCHIB | basic endochitinase | 1.4 | -0.1 | -0.3 | 0 | 0.4 | -0.3 | -0.1 | 0.3 | -0.3 | 0 | 0.2 | -0.3 | 0.1 | 1.4 | -0.6 | 0.6 | 0.3 | -0.4 | -0.1 | 0.4 | -0.6 | 0.8 | -0.3 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | 0 | -0.9 | 0 | -0.2 | -0.2 | -0.1 | 0 | 0.4 | 0.2 | 0.5 | 0.1 | 0 | 0.1 | 0.4 | 0.1 | 0.1 | 0.4 | 0.5 | 0 | 0.3 | 0 | 0 | 0.5 | -0.3 | -0.4 | -0.2 | -0.5 | 0 | -2.4 | 0 | -2.7 | 0.3 | -0.2 | 0.3 | -0.6 | 1.1 | -0.5 | -1.2 | 1.6 | -0.2 | -0.1 | 0.2 | 0.5 | 0 | 0 | -0.4 | -0.1 | 1.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | 0.5 | -0.2 | 0 | 0 | 0.2 | -0.3 | 0 | -0.1 | 0.1 | 0 | 0 | -0.2 | -0.1 | -0.1 | 2.7 | At3g12500 | 256243_at | ATHCHIB | basic endochitinase | 9 | chitinase activity | defense response to fungi | jasmonic acid and ethylene-dependent systemic resistance, ethylene mediated signaling pathway | Aminosugars metabolism | 1.78 | 5.51 | ||||||
| At2g34500 | 0.532 | CYP710A1 | cytochrome P450 family protein, similar to Cytochrome P450 61 (C-22 sterol desaturase) (Saccharomyces cerevisiae) | 0 | 0 | -0.1 | 0.5 | -0.6 | -0.1 | 0.2 | 0 | -0.1 | 0.3 | -0.5 | -0.4 | 0.7 | 1.4 | 0 | 0 | -0.1 | -1.2 | -0.1 | -1.4 | -0.1 | 0 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | -0.3 | -0.8 | 0 | -0.1 | 0 | -0.5 | -0.2 | 0.6 | 0 | 0.2 | -0.1 | 0 | 0 | 0.1 | 0.9 | 0.4 | 0.3 | 0.2 | -0.2 | 0 | 0 | 0.1 | 1 | 0.6 | 0.1 | -1 | -0.1 | 0.4 | 1.6 | -0.3 | 0.4 | -0.5 | 1 | 0 | 0 | 0 | 0.5 | 0.3 | 2 | -0.4 | 0 | 0.4 | 0.1 | 0 | 0 | 0.3 | -1.7 | -2.6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | -0.3 | 0 | 2.2 | At2g34500 | 266995_at | CYP710A1 | cytochrome P450 family protein, similar to Cytochrome P450 61 (C-22 sterol desaturase) (Saccharomyces cerevisiae) | 1 | cytochrome P450 family | 1.80 | 4.89 | |||||||
| At3g48690 | 0.530 | expressed protein, similar to PrMC3 (Pinus radiata) | 0 | -0.1 | -0.1 | -0.1 | 0.2 | -0.2 | -0.1 | -0.1 | 0 | 0 | -0.4 | 0.1 | 0.1 | 1.2 | 0 | 0 | 0.3 | -0.2 | -0.1 | -0.1 | -0.2 | -0.6 | -0.8 | -0.1 | 0 | 0.1 | 0.3 | 0.2 | 0.1 | 0.3 | 0.2 | 0 | -0.3 | -0.4 | -0.2 | 0 | -0.4 | -0.2 | 0.3 | 0.3 | 0.3 | 0.2 | 0.2 | 0.2 | 0.6 | 0.2 | 0.4 | 0.1 | 0 | 0 | 0.6 | 0 | 0.4 | 0 | 1.1 | 0 | 0.2 | 0 | 0.3 | 0.1 | 0.6 | 0.1 | -0.9 | -0.1 | 0.5 | 0.1 | -0.1 | -0.1 | 0 | 0 | 0.5 | 0 | 0 | -0.2 | 0 | 0 | -0.3 | 0.2 | -1.4 | -0.9 | -0.2 | -0.4 | -0.4 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | -0.2 | -0.4 | -0.2 | -0.1 | 0.1 | -0.2 | -0.5 | -0.2 | -0.2 | -0.2 | 0 | 0 | -0.3 | -0.1 | -0.1 | 0.7 | 2.1 | At3g48690 | 252315_at | expressed protein, similar to PrMC3 (Pinus radiata) | 2 | carboxylesterase | 1.13 | 3.54 | |||||||||
| At4g34710 | 0.530 | ADC2 | arginine decarboxylase 2 is the gene responsible for induction of the polyamine biosynthetic pathway by osmotic stress. | 0.1 | -0.1 | 0 | 0 | 0.4 | -0.1 | 0 | 0 | -0.1 | -0.1 | -0.1 | -0.1 | 0.3 | 1.4 | 0.2 | 0.6 | 1.6 | -0.3 | -0.3 | 0 | -0.3 | -0.5 | -0.6 | 0 | 0.1 | 0 | 0.4 | 0.1 | 0 | 0.4 | 0.1 | 0 | 0.3 | 0.1 | 0.1 | 0.5 | -0.1 | -0.3 | -0.1 | 0.1 | 0 | 0.1 | 0 | 0 | -0.3 | 0 | 0 | 0.1 | -0.4 | 0.1 | -0.2 | 0 | -0.1 | -0.1 | 0.8 | -0.2 | 0.5 | -0.4 | 0.1 | 0.2 | 0.7 | -0.2 | 0 | -0.9 | 0 | -0.6 | -0.2 | -0.3 | 0.5 | 0.5 | 2 | 0.6 | 0 | -0.2 | -0.2 | -0.2 | 0.2 | 0.8 | -1.1 | -0.7 | -1 | -0.7 | -0.5 | -0.3 | -0.3 | -0.2 | 0 | -0.4 | -0.4 | -0.1 | 0 | -0.2 | 0.2 | -0.1 | 0 | -0.2 | 0 | -0.2 | 0 | 0 | 0.1 | 0 | 0.2 | -0.3 | 1 | At4g34710 | 253203_at | ADC2 | arginine decarboxylase 2 is the gene responsible for induction of the polyamine biosynthetic pathway by osmotic stress. | 7 | embryonic development (sensu Magnoliophyta) | response to wounding | response to abscisic acid stimulus | response to jasmonic acid stimulus | seed development | arginine decarboxylase activity | response to osmotic stress | polyamine biosynthesis | putrescine biosynthesis | biosynthesis of secondary products derived from primary amino acids | biosynthesis of amines | spermine biosynthesis I | polyamine biosynthesis II | polyamine biosynthesis III | polyamine biosynthesis I | arginine degradation II | arginine degradation III | arginine degradation V | arginine degradation XII | Glutamate metabolism | Arginine and proline metabolism | 1.44 | 3.19 | ||||
| At5g13320 | 0.530 | similar to auxin-responsive GH3 product (Glycine max) | -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 | -0.1 | -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 | -0.5 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | 6.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | 4.8 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -3.8 | -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 | -0.1 | -0.1 | -0.1 | -0.1 | 4.7 | At5g13320 | 250286_at | similar to auxin-responsive GH3 product (Glycine max) | 4 | plant / fungal specific systemic sensing and response | plant hormonal regulation | plant development | Acyl activating enzymes , CoA ligases, clade III, putative hormone adenylase | 0.00 | 10.08 | ||||||||
| At4g35420 | 0.528 | dihydroflavonol 4-reductase family / dihydrokaempferol 4-reductase family | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0.1 | 0 | 0 | 0.1 | 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 | 0.6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0.2 | 0 | -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 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | At4g35420 | 253195_at | dihydroflavonol 4-reductase family / dihydrokaempferol 4-reductase family | 2 | biosynthesis of secondary products derived from L-phenylalanine and L-tyrosine | biosynthesis of phenylpropanoids | biosynthesis of stilbenes, flavonoids | anthocyanin biosynthesis | 0.21 | 2.28 | ||||||||
| At4g04020 | 0.527 | strong similarity to plastid-lipid associated proteins PAP1 (Brassica rapa), fibrillin (Brassica napus) | 0 | -0.1 | 0 | 0 | 0 | -0.1 | 0 | 0 | 0 | -0.1 | -0.3 | 0 | 0.3 | 1.6 | -0.1 | 0 | 0.1 | -0.2 | -0.2 | -0.2 | -0.1 | -0.3 | -0.1 | 0 | 0.3 | -0.2 | -0.4 | -0.9 | -0.2 | -0.4 | -0.9 | -0.3 | -0.4 | -0.6 | -0.1 | 0 | 0 | -0.3 | 0.3 | 0 | 0.3 | 0.2 | 0.1 | -0.1 | 0.2 | 0 | 0.1 | 0 | 0 | -0.2 | 0.5 | 0 | 0.3 | 0 | 0.6 | -0.2 | 0.3 | 0.3 | 0.3 | 0 | 0.6 | 0.2 | -1.6 | 0.3 | 0.2 | 0.2 | 0.2 | 0.3 | 0.3 | 0.3 | 1 | 0.3 | -0.3 | 0 | 0.1 | 0.2 | -0.1 | 0.5 | -0.3 | -0.6 | -0.4 | 0 | -0.1 | -0.1 | -0.1 | 0 | 0 | -0.1 | -0.2 | -0.5 | -0.3 | -0.2 | 0.2 | -0.2 | -0.2 | -0.1 | 0 | 0 | 0.1 | 0 | 0 | 0.2 | 0.3 | 0.5 | 1 | At4g04020 | 255364_s_at | strong similarity to plastid-lipid associated proteins PAP1 (Brassica rapa), fibrillin (Brassica napus) | 6 | transcription | Miscellaneous acyl lipid metabolism | 1.10 | 3.29 | ||||||||
| At2g29460 | 0.525 | ATGSTU4 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | 0.1 | -0.2 | -0.2 | -0.5 | 0.7 | -0.2 | -1.1 | -0.2 | -0.2 | -1.1 | -0.2 | -0.2 | -1.1 | 2.5 | -0.2 | 0.6 | 2 | -0.2 | -1.1 | 0.6 | -0.2 | -1.1 | -0.2 | 0 | 0 | -0.2 | -1 | -0.7 | -0.2 | -1 | -0.7 | 0 | 0.5 | 0.1 | 0.4 | 1 | -0.7 | 0.3 | -1.3 | -0.2 | -0.3 | 1.5 | -0.5 | 0.2 | -0.9 | 0.4 | -0.4 | 0.2 | 0.1 | 0.5 | 0.6 | 0.9 | -0.9 | -0.9 | 3.7 | -0.9 | 0.4 | -0.3 | 0.7 | 1 | 2 | -0.9 | -0.5 | -0.5 | 2.9 | -0.9 | 0.5 | -0.2 | 1 | 0.4 | 1.9 | -0.1 | 0.3 | 0.2 | -0.2 | -0.3 | 0.1 | 1.4 | -2.9 | -1.9 | -0.2 | -0.2 | -0.2 | -0.2 | -0.4 | -0.7 | -0.2 | -0.2 | -0.2 | -0.2 | -0.6 | -0.8 | -0.7 | -0.1 | -0.9 | -0.8 | -1.1 | -0.8 | 0 | 0.3 | -1.1 | 0.5 | 0.8 | 1.5 | 5.3 | At2g29460 | 266267_at | ATGSTU4 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | 2 | toxin catabolism | Glutathione metabolism | Glutathione S-transferase, Tau family | 3.16 | 8.23 | |||||
| At5g62480 | 0.525 | ATGSTU9 | Encodes glutathione transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | -0.1 | -0.1 | 0.4 | -1.2 | 0.9 | 0.2 | -1.2 | -0.2 | 0.6 | 0 | -0.3 | 0.2 | 0.9 | 2.9 | -0.6 | -1.2 | -1.4 | 0.4 | -0.2 | 0.4 | -0.6 | -0.4 | -0.1 | -0.1 | 0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.3 | -0.2 | -0.6 | -0.2 | 1 | 0 | 0.2 | -0.5 | 0.1 | -0.2 | -0.2 | -0.7 | -0.4 | -0.7 | 0 | -0.3 | 0.1 | -0.4 | -0.5 | 1.1 | -0.8 | -0.6 | -1.8 | -0.1 | -0.2 | 0.3 | 0.3 | -0.2 | -0.5 | 3 | 0 | 4.1 | -0.5 | 2 | -0.4 | -0.1 | -0.4 | -0.3 | -0.4 | 0.9 | 0.4 | -0.1 | 0.1 | 0.2 | 0.1 | 0 | -0.1 | -0.1 | -0.2 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.1 | -0.6 | 0 | -0.5 | 0 | -0.4 | -0.3 | -0.4 | -0.1 | 0 | 0 | 0 | -0.3 | -0.3 | 1.6 | -0.1 | 4 | At5g62480 | 247435_at | ATGSTU9 | 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 | 2.36 | 5.93 | ||||||
| At3g22840 | 0.523 | ELIP1 | chlorophyll A-B binding family protein / early light-induced protein (ELIP) | -0.1 | 0 | 0 | 0 | -0.3 | -0.7 | -0.3 | -0.2 | -0.5 | -0.2 | -0.1 | -0.3 | 0.3 | 1.6 | -0.5 | -0.6 | -1 | -0.3 | 0 | -0.2 | -0.3 | 0.1 | -0.2 | -0.7 | -1.3 | 0.1 | 0.2 | 0.4 | 0.1 | 0.2 | 0.4 | 0 | 0.2 | 1.5 | 0.3 | 0.4 | -0.2 | -1 | 0.6 | 0.3 | 0 | 0.1 | 0.5 | 0.3 | 0.2 | 0.1 | 0 | -0.2 | 0 | 0.4 | 0.1 | -0.2 | 0.9 | 0.2 | -0.5 | -0.1 | -0.3 | 0.3 | 0.4 | 0.5 | -0.5 | 0.5 | -1.5 | -0.8 | 0 | -0.8 | 0.2 | 1.2 | 0.2 | 0 | 1.4 | 0 | 0.4 | 0.2 | 0.7 | 0.7 | 0 | 0 | 1 | -0.2 | -0.8 | -1.1 | 0 | 0.2 | 0.1 | 0.1 | 0.2 | 0.1 | -0.2 | -2.8 | -3.3 | 0.1 | 2.2 | -0.3 | -2.4 | -0.4 | -1.3 | 0 | 1.3 | 0.8 | -3.3 | 1.4 | 0 | 0 | 6.1 | At3g22840 | 258321_at | ELIP1 | chlorophyll A-B binding family protein / early light-induced protein (ELIP) | 8 | Photosystems | additional photosystem II components | Early light-inducible proteins | 2.74 | 9.52 | |||||||
| At5g50320 | 0.518 | radical SAM domain-containing protein / GCN5-related N-acetyltransferase (GNAT) family protein | 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 | -0.2 | 0 | -0.1 | 0.3 | 0 | -0.1 | 0.3 | 0 | 0 | 0 | 0 | 0 | 0 | -0.4 | 0 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 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 | 0.2 | -0.1 | -0.1 | 0.4 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0.1 | -0.2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1.4 | At5g50320 | 248510_at | radical SAM domain-containing protein / GCN5-related N-acetyltransferase (GNAT) family protein | 2 | chlorophyll biosynthesis | biosynthesis of proto- and siroheme | 0.26 | 1.82 | |||||||||
| At1g65820 | 0.516 | putative microsomal glutathione s-transferase | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | 0 | 0 | 0 | 0 | 0 | 0.1 | 0 | 0 | 0.1 | 0 | -0.1 | 0 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | -0.2 | -0.6 | -0.1 | -0.2 | -0.6 | -0.2 | -0.2 | -0.4 | 0 | 0 | -0.2 | -0.5 | 0 | 0.1 | 0 | 0.2 | 0 | 0.1 | 0 | 0 | 0 | 0.1 | 0.1 | 0.1 | 0 | 0 | 0.2 | 0 | 0.6 | 0 | 0.1 | 0.1 | 0 | 0 | 0 | -0.1 | -0.5 | 0 | 0.1 | 0 | 0 | 0 | 0.1 | 0.2 | 1 | 0.3 | -0.1 | 0 | -0.1 | 0 | 0 | 0.3 | -0.2 | -0.2 | 0.3 | 0.1 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | 0 | 0 | -0.1 | 0 | 0.1 | 0.2 | 1 | At1g65820 | 262932_at | putative microsomal glutathione s-transferase | 4 | Glutathione metabolism | 0.54 | 1.68 | |||||||||
| At4g22260 | 0.516 | IM | Similar to mitochondrial alternative oxidase. im mutants have a variagated phenotype and fail to differentiate chloroplasts in the majority of their cells under high light intensity continuous illumination. The white tissues of immutans accumulate phytoe | 0 | 0 | 0 | -0.3 | 0 | 0 | -0.3 | -0.1 | 0 | -0.3 | 0 | -0.3 | -0.5 | 0 | -0.2 | -0.2 | 0 | -0.2 | -0.5 | -0.4 | -0.1 | -0.3 | -0.1 | -0.1 | 0 | 0 | -0.2 | 0 | 0 | -0.2 | 0 | -0.2 | 0.1 | -0.4 | -0.2 | -0.2 | -0.3 | -0.5 | 0.1 | 0 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0.2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.1 | 0 | -0.1 | 0.1 | -0.1 | 0.2 | 0 | 0 | 0 | 0 | 0 | 0.4 | 0.3 | 0.4 | 0.4 | 0.1 | 0 | 0.1 | 0.2 | 1.3 | 0.4 | 0 | -0.1 | 0 | 0 | 0 | 0.3 | -0.2 | -0.4 | -0.3 | 0.1 | 0.2 | 0.1 | 0 | 0 | 0 | -0.1 | 0 | -0.1 | 0.1 | 0 | 0.1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | -0.1 | 0 | 0.4 | 1.3 | At4g22260 | 254335_at | IM | Similar to mitochondrial alternative oxidase. im mutants have a variagated phenotype and fail to differentiate chloroplasts in the majority of their cells under high light intensity continuous illumination. The white tissues of immutans accumulate phytoe | 10 | carotenoid biosynthesis | plastid organization and biogenesis | response to high light intensity | response to temperature | Plastidial Isoprenoids (Chlorophylls, Carotenoids, Tocopherols, Plastoquinone, Phylloquinone) | Regulatory enzymes | Accessory protein/regulatory protein | 0.85 | 1.89 | |||||
| At2g33590 | 0.513 | similar to cinnamoyl-CoA reductase from Pinus taeda and Eucalyptus gunnii | 0 | 0 | 0 | 0 | 0.2 | 0 | -0.3 | -0.1 | 0 | -0.3 | 0 | 0.1 | 0.1 | 2.7 | -0.1 | -0.2 | 0 | 0 | -0.3 | 0.1 | 0 | 0 | 0.2 | 0.2 | 0.5 | -0.1 | -0.3 | -0.4 | -0.1 | -0.3 | -0.4 | 0.1 | 0.1 | -0.8 | 0.3 | 0.1 | 0 | -0.8 | -0.1 | -0.3 | -0.2 | -0.3 | 0 | -0.5 | 0 | -0.2 | -0.1 | -0.2 | -0.1 | -0.3 | 0.2 | -0.1 | 0 | 0 | 0.7 | 0 | 0.7 | 0 | -0.1 | 0.3 | 0.9 | 0.3 | 1.9 | 0.1 | 0.9 | -0.2 | -0.1 | 0.5 | 0.1 | 0.1 | 0.1 | -0.3 | 0 | -0.1 | 0 | 0.1 | -0.1 | 0.2 | -1.3 | -0.9 | 0 | -0.5 | -0.3 | 0 | -0.1 | -0.1 | 0.1 | -0.2 | 0 | -0.5 | -0.7 | -0.3 | 0.2 | -0.2 | -0.6 | -0.1 | -0.4 | 0 | 0.1 | 0.1 | -0.5 | 0.5 | 0.4 | 0.3 | 1.3 | At2g33590 | 255787_at | similar to cinnamoyl-CoA reductase from Pinus taeda and Eucalyptus gunnii | 4 | colanic acid building blocks biosynthesis | dTDP-rhamnose biosynthesis | galactose degradation I | UDP-glucose conversion | lactose degradation IV | Phenylpropanoid Metabolism | core phenylpropanoid metabolism | Phenylpropanoid pathway | 1.39 | 4.10 | |||||||
| At1g10370 | 0.512 | ATGSTU17, GST30B | ERD9 glutathione S-transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | 0 | 0 | -0.3 | 0 | -0.5 | 0 | -0.1 | 0 | -0.2 | 0.1 | 0 | -0.1 | 1.1 | 2.5 | -0.3 | -0.1 | 0 | 0 | 0.4 | 0 | -0.4 | 0.3 | 0.5 | -0.5 | -1.2 | 0 | 0.4 | 0.1 | 0 | 0.4 | 0.1 | -0.2 | -0.6 | -1.1 | 0 | -0.1 | -0.4 | -1 | 0.2 | -0.4 | 0.4 | -0.6 | 0.6 | -0.6 | 0.3 | -0.3 | 0 | -0.6 | 0 | 0 | 0.2 | -0.2 | 0.8 | 0.1 | 0.5 | 0.3 | -0.4 | 0.6 | 0.6 | 0 | 0.1 | 0.3 | -1.4 | -0.4 | 0 | -0.7 | -0.5 | 3.6 | -0.2 | -0.4 | 1 | -0.4 | 0.1 | 0.1 | 0.2 | 0.5 | 0.4 | -0.3 | -0.2 | -1 | -0.8 | -0.8 | -0.7 | 0 | 0 | 0 | 0.7 | 0 | 0 | -1.3 | -1.6 | -0.1 | 0.9 | -0.2 | -1.2 | -0.1 | -0.5 | -0.1 | 0.5 | 0.3 | -0.4 | 0.3 | 0.4 | 0.8 | 2.9 | At1g10370 | 264436_at | ATGSTU17, GST30B | ERD9 glutathione S-transferase belonging to the tau class of GSTs. Naming convention according to Wagner et al. (2002). | 2 | toxin catabolism | Glutathione S-transferase, Tau family | 2.04 | 5.36 | ||||||
| At5g65110 | 0.508 | ACX2 | Encodes an acyl-CoA oxidase presumably involved in long chain fatty acid biosynthesis. | -0.2 | 0 | -0.2 | 0 | 0.1 | 0 | 0 | -0.3 | -0.1 | 0.1 | 0 | 0 | 0.7 | 1.7 | -0.1 | 0 | -0.3 | 0 | 0.1 | 0 | 0 | 0.1 | -0.1 | -0.1 | 0 | 0.2 | 0.1 | 0.4 | 0.2 | 0.1 | 0.4 | 0 | 0.2 | -0.2 | -0.2 | -0.1 | -0.3 | -0.4 | -0.3 | 0 | -0.1 | 0 | -0.1 | 0.1 | 0 | 0.4 | 0.1 | 0.2 | -0.2 | -0.1 | 0 | 0 | -0.5 | -0.2 | 0.4 | 0 | 0 | -0.4 | -0.3 | -0.2 | 0.5 | 0 | -0.6 | 0 | 0.7 | 0 | -0.2 | 0 | 0.3 | 0.4 | -0.3 | -0.1 | 0 | 0 | -0.1 | 0 | -0.2 | 0.5 | 0 | -0.2 | 0 | -0.5 | -0.4 | -0.3 | -0.1 | 0 | -0.1 | 0.1 | 0.1 | 0 | 0.1 | 0 | -0.1 | 0 | 0 | 0 | -0.1 | -0.1 | -0.1 | 0 | 0 | -0.2 | 0.4 | 0 | 1.3 | At5g65110 | 247176_at | ACX2 | Encodes an acyl-CoA oxidase presumably involved in long chain fatty acid biosynthesis. | 10 | acyl-CoA oxidase activity | long-chain fatty acid metabolism | Fatty acid metabolism | Gluconeogenesis from lipids in seeds | fatty acid beta oxidation complex | Degradation of storage lipids and straight fatty acids | 0.96 | 2.40 | ||||
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