|
|
|
magnitude of change |
0 |
0.3 |
0.6 |
0.9 |
1.2 |
1.5 |
1.8 |
2.1 |
2.4 |
2.7 |
>2.99 |
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greater than zero |
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less than zero |
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Locus |
r-value |
Name |
Description |
suspension cell, aphidicolin, 0h ( 5) |
suspension cell, aphidicolin, 2h (5) |
suspension cell, aphidicolin, 4h (5) |
suspension cell, aphidicolin, 6h (5) |
suspension cell, aphidicolin, 8h (5) |
suspension cell, aphidicolin, 10h (5) |
suspension cell, aphidicolin, 12h (5) |
suspension cell, aphidicolin, 14h (5) |
suspension cell, aphidicolin, 16h (5) |
suspension cell, aphidicolin, 19h (5) |
suspension cell, sucrose, 0h (6) |
suspension cell, sucrose, 2h (6) |
suspension cell, sucrose, 4h (6) |
suspension cell, sucrose, 6h (6) |
suspension cell, sucrose, 8h (6) |
suspension cell, sucrose, 10h (6) |
suspension cell, sucrose, 12h (6) |
suspension cell, 1d (19) |
suspension cell, 1d (19) |
suspension cell, 5d (19) |
suspension cell, 7d (19) |
suspension cell, senescing (20) |
protoplast (62) |
suspension cell, light (153) |
suspension cell, dark (153) |
callus, transdifferentiation A1 (78) |
callus, transdifferentiation A2 (78) |
callus, transdifferentiation A3 (78) |
callus, transdifferentiation A4 (78) |
callus, transdifferentiation A5 (78) |
callus, transdifferentiation A6 (78) |
seedling (59) |
seedling (137) |
seedling (138) |
seedling (143) |
seedling (144) |
seedling, cont. light, 26h (149) |
seedling, cont. light, 26h (149) |
seedling, cont. light, 34h (149) |
seedling, cont. light, 38h (149) |
seedling, cont. light, 42h (149) |
seedling, cont. light, 46h (149) |
seedling, cont. light, 50h (149) |
seedling, cont. light, 54h (149) |
seedling, cont. light, 58h (149) |
seedling, cont. light, 62h (149) |
seedling, cont. light, 66h (149) |
seedling, cont. light, 70h (149) |
seedling, cont. light, 74h (149) |
seedling, far red then white light (83) |
seedling, dark then white light (83) |
Cotyledon (87) |
Hypocotyl (87) |
Hypocotyl (139) |
leaf, dedifferentiation A01 (50) |
leaf, dedifferentiation A02 (50) |
leaf, dedifferentiation A81 (50) |
leaf, dedifferentiation A82 (50) |
leaf, dedifferentiation A301 (50) |
leaf, dedifferentiation A302 (50) |
leaf, dedifferentiation A481 (50) |
leaf, dedifferentiation A482 (50) |
leaf, dedifferentiation B01 (50) |
leaf, dedifferentiation B02 (50) |
leaf, whole rosette, 0h (56) |
leaf, whole rosette, 0h (56) |
leaf, whole rosette, 2h (56) |
leaf, whole rosette, 4h (56) |
leaf, whole rosette, 8h (56) |
leaf, whole rosette, 12h (56) |
leaf, whole rosette, 13h (56) |
leaf, whole rosette, 14h (56) |
leaf, whole rosette, 16h (56) |
leaf, whole rosette, 20h (56) |
leaf, whole rosette, 24h (56) |
leaf, whole rosette, 0h (56) |
leaf, whole rosette, 4h (56) |
leaf, whole rosette, 8h (56) |
leaf, whole rosette, 12h (56) |
leaf, whole rosette, 16h (56) |
leaf, whole rosette, 20h (56) |
leaf, mature, high light (68) |
leaf, mature, low light (68) |
leaf stage 7, petiol (88) |
leaf stage 7, proximal half (88) |
leaf stage 7, distal half (88) |
guard cell enriched (11) |
senescing leaf, Col5 (60) |
senescing leaf, Col0 (60) |
senescing leaf (88) |
cauline leaf (88) |
roots (87) |
whole roots, A. halleri (101) |
whole roots, A. petrea (101) |
roots (141) |
mature roots (23) |
lateral roots (24) |
lateral roots (29) |
roots, axillary buds, dormant (30) |
roots, axillary buds, active (30) |
Roots, N03 depleted, dex treated (64) |
Roots, N03 depleted (64) |
root elongation zone (79) |
stem (80) |
stem (88) |
stem, base (66) |
stem, tip (66) |
stem, 1st node (88) |
stem, base, injured with needle (8) |
shoot apex (87) |
shoot apex (87) |
shoot apex (88) |
apical region, vegetative, Col (94) |
apical region, reproductive, 3d, Col (94) |
apical region, reproductive, 5d, Col (94) |
apical region, reproductive, 7d, Col (94) |
apical region, vegetative, Ler (94) |
apical region, reproductive, 3d, Ler (94) |
apical region, reproductive, 5d, Ler (94) |
apical region, reproductive, 7d, Ler (94) |
flower, stage 9 (89) |
flower, stage 10 (89) |
flower, stage 12 (89) |
flower, stage 15 (89) |
flower-silique, stage I (84) |
flower-silique, stage II (84) |
flower-silique, stage III (84) |
flower bud, young (9) |
flower bud, old (9) |
flower (80) |
flower (92) |
flower (100) |
sepal, stage 12 (89) |
sepal, stage 15 (89) |
petal, stage 12 (89) |
petal, stage 15 (89) |
stamen, stage 12 (89) |
stamen, stage 15 (89) |
carpel, stage 12 (89) |
carpel, stage 15 (89) |
pedicel, stage 15 (89) |
pollen, uninucleate microspores (22) |
pollen, bicellular (22) |
pollen, tricellular (22) |
pollen, mature (22) |
pollen (74) |
silique, young (136) |
silique, old (136) |
silique, stage 3 (90) |
silique, stage 4 (90) |
silique, stage 5 (90) |
seed, stage 6 (90) |
seed, stage 7 (90) |
seed, stage 8 (90) |
seed, stage 9 (90) |
seed, stage 10 (90) |
seed, dry (116) |
seed, dry (117) |
seed, fresh (96) |
seed, dormant (96) |
seed, imbibed, 1h (117) |
seed, imbibed, 3h (117) |
seed, imbibed, 22°C (118) |
seed, imbibed, far red, 22°C (132) |
seed, imbibed, 4°C (118) |
seed, imbibed, far red, 4°C (132) |
seed, imbibed (116) |
Locus |
Probeset |
Name |
Description |
Annotation score |
GO.keywords |
FunCat keywords |
AraCyc annotations |
KEGG annotations |
BioPath annotations |
AcylLipid category |
Literature annotations |
Gene family |
90% quantile of DE |
max. DE |
At2g30490 |
1.000 |
C4H, CYP73A5 |
trans-cinnamate 4-monooxygenase / cinnamic acid 4-hydroxylase (C4H) (CA4H) / cytochrome P450 73 (CYP73A5) |
-0.5 |
-0.4 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.8 |
-0.5 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.2 |
-1.3 |
2.4 |
0.8 |
-0.3 |
-0.4 |
0.6 |
1.3 |
1.5 |
1.3 |
1.5 |
1.2 |
0 |
2.5 |
-0.5 |
-0.3 |
0.2 |
0.6 |
0.4 |
0.2 |
0 |
0 |
0.4 |
0.7 |
0.2 |
-0.1 |
0.2 |
0.3 |
-0.6 |
0.5 |
0.9 |
0.2 |
0.1 |
0.1 |
2.3 |
0.1 |
-0.1 |
0.1 |
0.7 |
1 |
0.9 |
3 |
2.5 |
3.3 |
2.1 |
0.7 |
0.8 |
1.4 |
1.3 |
1.4 |
1.1 |
0.9 |
1.4 |
1.1 |
0.5 |
1 |
0.7 |
0.3 |
0.2 |
0.3 |
0.4 |
0.2 |
0.5 |
0.9 |
-0.1 |
0 |
0.3 |
1.6 |
1.9 |
1.9 |
2.4 |
0.8 |
-0.9 |
1.4 |
0.2 |
0.5 |
0.9 |
0.3 |
0 |
-0.4 |
-0.4 |
2.2 |
1.9 |
0.1 |
0 |
2.1 |
1.1 |
-1.1 |
0.6 |
1.6 |
-1.3 |
-1.5 |
-2 |
-1.9 |
-1.8 |
-1.8 |
-1.3 |
-1.5 |
-2 |
-1.3 |
-1.3 |
-1.7 |
-0.8 |
0 |
1.1 |
-0.6 |
0.2 |
0.3 |
-0.5 |
0 |
-1 |
-1.1 |
-1.3 |
1.1 |
2.1 |
0 |
1.7 |
-1 |
0.1 |
-1.8 |
-1.4 |
0.2 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
1.3 |
0.8 |
0 |
0.8 |
0.1 |
-0.8 |
-0.4 |
0.7 |
0.1 |
0.4 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.2 |
-1.2 |
-1.3 |
-1.3 |
-1.7 |
At2g30490 |
267470_at |
C4H, CYP73A5 |
trans-cinnamate 4-monooxygenase / cinnamic acid 4-hydroxylase (C4H) (CA4H) / cytochrome P450 73 (CYP73A5) |
10 |
trans-cinnamate 4-monooxygenase activity | response to light | response to wounding | phenylpropanoid biosynthesis |
|
suberin biosynthesis | lignin biosynthesis | phenylpropanoid pathway, initial reactions |
Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
cytochrome P450 family, cinnamic acid 4-hydroxylase, phenylpropanoid metabolism |
3.85 |
5.41 |
At1g52760 |
0.779 |
|
esterase/lipase/thioesterase family protein, low similarity to monoglyceride lipase from (Homo sapiens, Mus musculus) |
0.7 |
2.2 |
1.6 |
0.9 |
0.7 |
0.7 |
0.6 |
0.7 |
0.8 |
0.6 |
2.1 |
2.8 |
2.6 |
2.6 |
2 |
1.4 |
0.4 |
0 |
0.8 |
1.3 |
2 |
1.2 |
2.3 |
0.6 |
0.5 |
1.4 |
1.3 |
1.3 |
1.4 |
1.1 |
1.2 |
0.8 |
0.8 |
0.9 |
-1.6 |
0.5 |
0.5 |
0.5 |
0 |
0.3 |
0.6 |
0.4 |
0.4 |
0.2 |
0.3 |
0.4 |
0.5 |
0.2 |
0.2 |
1 |
0.5 |
-1 |
0.6 |
-0.9 |
-1.1 |
-1.1 |
0.3 |
0.1 |
-0.4 |
-1.2 |
0.7 |
0.6 |
1.5 |
1.2 |
-0.5 |
-0.8 |
-0.3 |
0 |
-0.5 |
-0.8 |
-0.6 |
-0.2 |
-0.8 |
-1 |
-0.8 |
0.2 |
-0.6 |
-0.7 |
-0.4 |
-0.3 |
-0.5 |
-0.2 |
-0.5 |
-0.6 |
-1 |
-1 |
-0.9 |
-0.5 |
-0.5 |
0 |
-0.3 |
1.3 |
-0.8 |
-2 |
1.7 |
1.6 |
0.8 |
2.1 |
-0.8 |
-0.4 |
1.7 |
1.6 |
2 |
1.7 |
2.6 |
0.7 |
-1.2 |
1.6 |
1 |
-0.3 |
-0.1 |
0.4 |
0.3 |
0.4 |
0.5 |
0.6 |
-1.7 |
-1.2 |
-1.5 |
-1.5 |
0.3 |
0 |
0.7 |
-0.3 |
-1.4 |
-2.5 |
-1.7 |
-1.7 |
-1.9 |
-0.2 |
0.1 |
-0.6 |
-0.5 |
-0.1 |
0.9 |
-2 |
1 |
-1.7 |
-0.3 |
0 |
0.3 |
-3.4 |
-3.4 |
-3.4 |
-3.4 |
-3.4 |
1 |
0 |
0.1 |
1.1 |
0.9 |
1.2 |
1.2 |
0.4 |
-0.2 |
-0.4 |
-1.3 |
-1.2 |
-2.4 |
-2.3 |
-1.1 |
-1.4 |
-1.9 |
-1.9 |
-3.3 |
-3.4 |
-1.1 |
At1g52760 |
260153_at |
|
esterase/lipase/thioesterase family protein, low similarity to monoglyceride lipase from (Homo sapiens, Mus musculus) |
2 |
|
|
|
|
|
Degradation of storage lipids and straight fatty acids |
|
|
4.50 |
6.26 |
At3g06300 |
0.697 |
|
Encodes a prolyl-4 hydroxylase that can hydroxylate poly(L-proline)and other proline rich peptides, including those with sequences corresponding to those in arabinogalactan proteins and extensins. |
-0.1 |
0.5 |
0.1 |
-0.1 |
-0.2 |
-0.2 |
-0.1 |
0 |
-0.3 |
0 |
0.2 |
0.7 |
0.4 |
0.2 |
0 |
0.1 |
-0.2 |
-0.1 |
-0.1 |
0.3 |
0.7 |
0 |
0.4 |
0.6 |
-0.6 |
0.7 |
0.3 |
0.1 |
0.5 |
0.6 |
0.6 |
0 |
1 |
0.5 |
0.4 |
0.6 |
0.4 |
0.5 |
0 |
0.3 |
0.2 |
0 |
0.1 |
0 |
0.1 |
0 |
0.1 |
0.2 |
0 |
-0.3 |
0 |
-0.6 |
0.3 |
0.5 |
-0.8 |
-0.4 |
0.9 |
0.7 |
0 |
-0.3 |
0.7 |
1.2 |
0.3 |
0.8 |
0 |
-0.2 |
0.2 |
0 |
-0.4 |
-0.6 |
-0.7 |
-0.7 |
-0.5 |
-0.2 |
0 |
-0.1 |
-1.2 |
-0.8 |
-0.7 |
-1 |
-1 |
-1.5 |
-1.2 |
-0.3 |
-0.4 |
-0.6 |
-0.4 |
0.2 |
0 |
0 |
-0.6 |
1.6 |
2.1 |
2 |
2.3 |
1.9 |
1 |
2.9 |
-1 |
-0.7 |
2.3 |
2.2 |
2.8 |
0.8 |
0.8 |
1.3 |
0.4 |
0.8 |
0.3 |
-0.3 |
0 |
0 |
0 |
0 |
0 |
0 |
0.1 |
0.1 |
0.3 |
0.4 |
0.9 |
0.3 |
0 |
-0.2 |
0.3 |
-0.7 |
0 |
0.3 |
-0.2 |
0 |
0.5 |
-0.3 |
-1 |
-0.9 |
0.2 |
-1.3 |
-0.8 |
-0.9 |
0.2 |
0 |
0.2 |
-0.3 |
-0.6 |
-1.8 |
-1.8 |
-1.8 |
0 |
-0.3 |
-0.2 |
0.3 |
0.3 |
0.3 |
0.1 |
-0.7 |
-1.2 |
-0.9 |
-2.1 |
-1.8 |
-0.6 |
0.7 |
-2.3 |
-2.3 |
-0.2 |
-0.2 |
-2.1 |
-2.1 |
-0.1 |
At3g06300 |
258852_at |
|
Encodes a prolyl-4 hydroxylase that can hydroxylate poly(L-proline)and other proline rich peptides, including those with sequences corresponding to those in arabinogalactan proteins and extensins. |
6 |
procollagen-proline 4-dioxygenase activity | peptidyl-proline hydroxylation to 4-hydroxy-L-proline |
|
|
|
Biosynthesis of Amino Acids and Derivatives | Prolin/Hydroxyproline from glutamate |
|
|
|
3.26 |
5.32 |
At4g34050 |
0.696 |
CCOMT |
caffeoyl-CoA 3-O-methyltransferase |
-0.7 |
0.5 |
1 |
0.1 |
-1.3 |
-1.8 |
-1.9 |
-1.6 |
-1.2 |
-1.9 |
0.1 |
2.1 |
2 |
1.8 |
1.1 |
0.5 |
-1.5 |
-3.9 |
-2.9 |
-1.2 |
0.6 |
-1.6 |
1.5 |
1 |
-0.3 |
1.1 |
0.1 |
0.3 |
0.9 |
0.1 |
0.4 |
0.6 |
0.9 |
1 |
0.8 |
0.9 |
0.6 |
0.4 |
0.4 |
0.5 |
0.8 |
0.8 |
0.8 |
0.2 |
0.5 |
0.6 |
0.6 |
0.6 |
0.7 |
-0.2 |
0 |
0 |
0.4 |
0.3 |
1.2 |
0 |
0.9 |
1.1 |
-0.1 |
-0.1 |
1.6 |
1.6 |
1.9 |
1.7 |
0.1 |
-0.5 |
-0.1 |
0.1 |
-0.2 |
-0.5 |
-0.2 |
0.3 |
0.5 |
0.4 |
0 |
0.3 |
0.3 |
-0.1 |
0.3 |
-0.1 |
-0.1 |
0.5 |
0.5 |
0 |
0 |
-0.2 |
0 |
0.4 |
0.3 |
0.1 |
0 |
1.2 |
1.5 |
0.9 |
1.6 |
1.5 |
1 |
1.9 |
-1 |
-0.4 |
1.8 |
1.7 |
1.9 |
2.6 |
2.4 |
2.5 |
0.5 |
1.7 |
1 |
-0.2 |
-0.5 |
-0.3 |
-0.6 |
-0.4 |
-0.5 |
-0.1 |
0.5 |
0.5 |
0.1 |
0.3 |
0.4 |
0.4 |
0.5 |
0 |
0.8 |
0.6 |
0.5 |
0.1 |
0 |
0 |
0.1 |
-0.5 |
0.2 |
0.6 |
0.5 |
-0.5 |
1.1 |
0.3 |
-0.9 |
-0.4 |
0 |
-3.9 |
-3.9 |
-3.9 |
-3.9 |
-3.9 |
1.4 |
0.7 |
0 |
1.7 |
1.3 |
1.2 |
1.5 |
0.2 |
0.2 |
-0.6 |
-3.9 |
-3.9 |
-3.9 |
-3.7 |
-3.9 |
-3.9 |
-0.3 |
-0.3 |
-3.5 |
-3.2 |
-3.9 |
At4g34050 |
253276_at |
CCOMT |
caffeoyl-CoA 3-O-methyltransferase |
10 |
|
biogenesis of cell wall |
suberin biosynthesis | lignin biosynthesis |
Stilbene, coumarine and lignin biosynthesis |
|
|
Phenylpropanoid pathway |
Methyltransferase, CCOMT like |
5.81 |
6.54 |
At5g48930 |
0.695 |
HCT |
Hydroxycinnamoyl-CoA:shikimate/quinate hydroxycinnamoyltransferase |
-1.3 |
2 |
0 |
-0.7 |
-0.8 |
-0.9 |
-1.2 |
-1 |
-1.1 |
-1.2 |
1.1 |
2.8 |
2.2 |
1.7 |
0.8 |
0 |
-1.3 |
-1.2 |
-1 |
-0.1 |
0.8 |
0.1 |
1.5 |
0.2 |
-0.8 |
0.4 |
-0.9 |
-0.5 |
0.2 |
-0.2 |
-0.1 |
0.7 |
0.6 |
0.7 |
0.2 |
0.2 |
0.7 |
0.4 |
0.2 |
0.5 |
0.6 |
0.6 |
0.5 |
0.2 |
0.1 |
0.5 |
0.6 |
0.6 |
0.6 |
-0.2 |
0.3 |
0.2 |
0.3 |
-0.1 |
1.1 |
0.4 |
0.6 |
0.8 |
1.3 |
0.7 |
1 |
1.1 |
1.8 |
1.6 |
-0.2 |
-0.4 |
0.2 |
0.3 |
0.3 |
0.6 |
0.2 |
0.6 |
0.6 |
0 |
-0.4 |
0.9 |
0.8 |
0 |
0 |
0.2 |
0.7 |
0.5 |
0.6 |
0.2 |
0 |
0 |
0.2 |
0 |
0.1 |
-0.2 |
-0.3 |
0.5 |
-0.7 |
-1.4 |
0.8 |
1.5 |
1.1 |
1.4 |
-0.6 |
-0.1 |
1.3 |
1.3 |
1.4 |
0.9 |
2.2 |
2 |
-0.1 |
1.5 |
1.7 |
-0.6 |
-0.6 |
-0.9 |
-0.7 |
-0.7 |
-0.8 |
-0.8 |
-0.5 |
-1 |
-1 |
-1 |
-0.9 |
-0.8 |
0 |
-0.3 |
-0.1 |
-0.8 |
-0.3 |
-0.7 |
-0.6 |
-1.1 |
-0.8 |
-1 |
-0.3 |
0.2 |
-0.5 |
-0.9 |
0.6 |
-0.2 |
-1.3 |
-0.9 |
-0.3 |
-2.2 |
-2 |
-1.9 |
-2.1 |
-1.7 |
0.9 |
-0.1 |
-0.2 |
0.8 |
0.3 |
0.7 |
0.9 |
0 |
0.2 |
-0.3 |
-1.1 |
-0.9 |
-0.5 |
-1.6 |
-1 |
-1.2 |
0 |
0 |
-1.7 |
-1.8 |
-2.6 |
At5g48930 |
248639_at |
HCT |
Hydroxycinnamoyl-CoA:shikimate/quinate hydroxycinnamoyltransferase |
10 |
|
|
|
|
|
|
Phenylpropanoid pathway |
acyltransferase, BAHD family, group D, HCT |
3.20 |
5.49 |
At2g40890 |
0.690 |
C3'H, CYP98A3 |
encodes coumarate 3-hydroxylase (C3H), a P450-dependent monooxygenase. Involved in lignin biosynthesis. |
-0.4 |
1.9 |
1.3 |
0.2 |
-0.2 |
-0.5 |
-0.5 |
-0.6 |
-0.5 |
-0.9 |
1.3 |
2.5 |
2.1 |
1.8 |
1.3 |
0.4 |
-1 |
-1.4 |
-1 |
-0.6 |
0.6 |
0.1 |
1.9 |
0.7 |
0 |
0.5 |
-0.3 |
-0.5 |
0 |
-0.5 |
-0.6 |
0.7 |
0.2 |
0.8 |
0.6 |
0.1 |
0.5 |
0.5 |
0.1 |
0.3 |
0.4 |
0.4 |
0.3 |
0.2 |
0 |
0.1 |
0.3 |
0.1 |
0.4 |
0.7 |
0.6 |
-0.9 |
0.1 |
-0.5 |
0.3 |
-0.4 |
0 |
0.5 |
-0.3 |
-0.4 |
0.6 |
0.8 |
1.2 |
1.1 |
-0.9 |
-1.1 |
-0.7 |
-0.5 |
-0.5 |
-0.2 |
-0.6 |
-0.4 |
-0.7 |
-0.8 |
-1.1 |
0.2 |
-0.3 |
-0.7 |
-0.9 |
-0.3 |
-0.1 |
-0.7 |
-0.5 |
-0.8 |
-1.3 |
-1.4 |
-0.2 |
-1.1 |
-0.7 |
-0.9 |
-0.8 |
0.4 |
1.3 |
0.9 |
1.2 |
1.5 |
0.1 |
2.2 |
-0.6 |
-0.2 |
1.8 |
1.8 |
2.2 |
1.4 |
2 |
2.2 |
0 |
1.4 |
0.7 |
-0.7 |
-0.4 |
-0.1 |
-0.8 |
-0.6 |
-0.8 |
-0.7 |
-0.2 |
-0.2 |
-0.3 |
-0.3 |
-0.5 |
-0.8 |
-0.1 |
-1.3 |
-0.2 |
-1.1 |
-0.5 |
-0.1 |
-0.5 |
-0.8 |
-0.5 |
-0.6 |
-0.6 |
-0.4 |
-1.4 |
-2.2 |
0.5 |
-2.6 |
-1.4 |
-1.2 |
-0.5 |
-1.1 |
-1.1 |
-1.1 |
-1.1 |
-1.1 |
0.4 |
-0.2 |
-1 |
0.3 |
0.1 |
0.4 |
0.8 |
1.3 |
1.3 |
1.4 |
1 |
1.1 |
0.5 |
-0.1 |
1.1 |
1.6 |
0.4 |
0.4 |
-0.1 |
-0.2 |
-0.4 |
At2g40890 |
245101_at |
C3'H, CYP98A3 |
encodes coumarate 3-hydroxylase (C3H), a P450-dependent monooxygenase. Involved in lignin biosynthesis. |
10 |
p-coumarate 3-hydroxylase activity | monooxygenase activity | phenylpropanoid biosynthesis | lignin biosynthesis |
|
suberin biosynthesis | lignin biosynthesis | phenylpropanoid biosynthesis |
Ascorbate and aldarate metabolism | Stilbene, coumarine and lignin biosynthesis | gamma-Hexachlorocyclohexane degradation | Fluorene degradation |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
cytochrome P450 family, 3’-hydroxylase for p-coumaryl shikimic/quinic acids, phenylpropanoid metabolism |
3.11 |
5.16 |
At1g51680 |
0.651 |
4CL1 |
encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it also converts ferulate. |
-3 |
3.1 |
2 |
0.9 |
-0.2 |
-0.7 |
-0.5 |
0.1 |
0.4 |
-0.9 |
2.5 |
3.3 |
3.3 |
3.5 |
3 |
2.4 |
0.9 |
-2.5 |
-3.1 |
0.4 |
1.8 |
1.1 |
3.1 |
0.8 |
-1.6 |
0.2 |
-1.6 |
-1.4 |
-0.2 |
-0.7 |
-0.8 |
1.3 |
0.7 |
1.3 |
0.8 |
0.1 |
1 |
0.4 |
0.3 |
0.6 |
0.9 |
0.9 |
0.9 |
0.4 |
0.5 |
0.9 |
1.1 |
0.9 |
0.8 |
-0.8 |
-0.4 |
0.3 |
0.6 |
-0.5 |
0.5 |
-1 |
1 |
0.8 |
0.9 |
0.2 |
1.6 |
1.1 |
2.1 |
1.1 |
0.2 |
-0.1 |
0.3 |
0.2 |
0.1 |
0 |
0.3 |
1.3 |
0.4 |
-0.2 |
0 |
0.7 |
0.5 |
-0.2 |
0.1 |
0.4 |
0.3 |
1.1 |
1.2 |
-0.1 |
0 |
-0.2 |
-0.3 |
0 |
-0.1 |
0.1 |
-0.4 |
0.8 |
-0.6 |
-1.5 |
1 |
1.5 |
0.7 |
1.9 |
-1.8 |
-0.9 |
1.7 |
1.7 |
1.9 |
1.3 |
2.9 |
2.9 |
-0.3 |
1.6 |
1.8 |
-0.6 |
-0.8 |
-2.4 |
-1.4 |
-1.7 |
-2 |
-2.6 |
-0.1 |
-1 |
-1.8 |
-1.8 |
-0.8 |
-0.9 |
0.1 |
0.4 |
0.1 |
0.6 |
0 |
-0.5 |
-0.3 |
-1.4 |
-0.6 |
-1.2 |
-0.2 |
0.4 |
0.8 |
1.4 |
0.9 |
1.2 |
-1.4 |
-0.6 |
-0.4 |
-3.7 |
-3.7 |
-3.7 |
-3.7 |
-3.7 |
1.1 |
-0.9 |
-0.8 |
1 |
0.3 |
0.5 |
0.3 |
-0.5 |
-0.9 |
-0.8 |
-1.4 |
-1.1 |
-1.1 |
-3.7 |
-0.9 |
-1.8 |
-0.2 |
-0.2 |
-3.7 |
-3.7 |
-4.3 |
At1g51680 |
256186_at |
4CL1 |
encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it also converts ferulate. |
10 |
4-coumarate-CoA ligase activity | response to UV | response to pathogenic fungi | response to wounding | phenylpropanoid metabolism |
|
lignin biosynthesis | flavonoid biosynthesis |
Stilbene, coumarine and lignin biosynthesis |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase |
6.07 |
7.82 |
At1g48860 |
0.646 |
|
Strong similarity to 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase from Arabidopsis thaliana |
1.2 |
2.4 |
2.2 |
1.5 |
1.4 |
1.4 |
1.4 |
1.3 |
1.5 |
1.4 |
0.8 |
2.5 |
2.4 |
2.3 |
2 |
1.7 |
1.3 |
1.2 |
1.3 |
1.2 |
1.4 |
0.4 |
2.7 |
0.4 |
-0.1 |
0.3 |
-0.1 |
-0.3 |
-0.1 |
-0.4 |
-0.1 |
0.3 |
0 |
0.1 |
-0.2 |
-0.1 |
0 |
0 |
0 |
0.2 |
0.3 |
0.4 |
0.3 |
0 |
0.2 |
0.4 |
0.3 |
0.3 |
0.1 |
0 |
0.3 |
-0.6 |
0.1 |
-0.8 |
-0.8 |
-0.6 |
1.1 |
0.6 |
0.1 |
-0.4 |
0.3 |
0.5 |
0.2 |
0.4 |
-0.2 |
-0.4 |
-0.2 |
-0.1 |
-0.3 |
-0.2 |
-0.2 |
0 |
0 |
-0.4 |
-0.5 |
0.2 |
0.2 |
0 |
-0.1 |
0 |
0 |
0.4 |
0.2 |
-0.7 |
-1 |
-1 |
-0.4 |
-0.8 |
-0.8 |
-0.9 |
-1 |
0.2 |
0.3 |
0 |
0.6 |
0.8 |
-0.5 |
0.6 |
-0.9 |
-0.9 |
0.7 |
0.8 |
0.7 |
-0.2 |
0.4 |
0.2 |
-0.3 |
0.1 |
0 |
0.1 |
0.3 |
0.2 |
0.1 |
0.1 |
0.4 |
0.1 |
0 |
0.1 |
0.2 |
0.2 |
0.1 |
-0.3 |
-0.3 |
-0.3 |
-0.2 |
0.1 |
-0.2 |
-0.3 |
-0.4 |
-0.7 |
-0.1 |
-0.5 |
-0.8 |
-0.7 |
-0.2 |
-0.6 |
-0.6 |
-0.5 |
-0.3 |
-0.2 |
-0.4 |
-1.3 |
-1.1 |
-2.1 |
-1.9 |
-1.6 |
-0.7 |
-1.1 |
-0.5 |
0 |
-0.4 |
-0.4 |
-0.6 |
-1.2 |
-1.3 |
-1.7 |
-1.9 |
-1.4 |
-1.2 |
-0.5 |
-1.6 |
-1 |
-1.2 |
-1.2 |
-0.6 |
-0.9 |
-0.3 |
At1g48860 |
246627_s_at (m) |
|
Strong similarity to 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase from Arabidopsis thaliana |
6 |
glyphosate metabolism | aromatic amino acid family biosynthesis, shikimate pathway |
|
chorismate biosynthesis |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
2.90 |
4.89 |
At2g45300 |
0.646 |
|
3-phosphoshikimate 1-carboxyvinyltransferase / 5-enolpyruvylshikimate-3-phosphate / EPSP synthase |
1.2 |
2.4 |
2.2 |
1.5 |
1.4 |
1.4 |
1.4 |
1.3 |
1.5 |
1.4 |
0.8 |
2.5 |
2.4 |
2.3 |
2 |
1.7 |
1.3 |
1.2 |
1.3 |
1.2 |
1.4 |
0.4 |
2.7 |
0.4 |
-0.1 |
0.3 |
-0.1 |
-0.3 |
-0.1 |
-0.4 |
-0.1 |
0.3 |
0 |
0.1 |
-0.2 |
-0.1 |
0 |
0 |
0 |
0.2 |
0.3 |
0.4 |
0.3 |
0 |
0.2 |
0.4 |
0.3 |
0.3 |
0.1 |
0 |
0.3 |
-0.6 |
0.1 |
-0.8 |
-0.8 |
-0.6 |
1.1 |
0.6 |
0.1 |
-0.4 |
0.3 |
0.5 |
0.2 |
0.4 |
-0.2 |
-0.4 |
-0.2 |
-0.1 |
-0.3 |
-0.2 |
-0.2 |
0 |
0 |
-0.4 |
-0.5 |
0.2 |
0.2 |
0 |
-0.1 |
0 |
0 |
0.4 |
0.2 |
-0.7 |
-1 |
-1 |
-0.4 |
-0.8 |
-0.8 |
-0.9 |
-1 |
0.2 |
0.3 |
0 |
0.6 |
0.8 |
-0.5 |
0.6 |
-0.9 |
-0.9 |
0.7 |
0.8 |
0.7 |
-0.2 |
0.4 |
0.2 |
-0.3 |
0.1 |
0 |
0.1 |
0.3 |
0.2 |
0.1 |
0.1 |
0.4 |
0.1 |
0 |
0.1 |
0.2 |
0.2 |
0.1 |
-0.3 |
-0.3 |
-0.3 |
-0.2 |
0.1 |
-0.2 |
-0.3 |
-0.4 |
-0.7 |
-0.1 |
-0.5 |
-0.8 |
-0.7 |
-0.2 |
-0.6 |
-0.6 |
-0.5 |
-0.3 |
-0.2 |
-0.4 |
-1.3 |
-1.1 |
-2.1 |
-1.9 |
-1.6 |
-0.7 |
-1.1 |
-0.5 |
0 |
-0.4 |
-0.4 |
-0.6 |
-1.2 |
-1.3 |
-1.7 |
-1.9 |
-1.4 |
-1.2 |
-0.5 |
-1.6 |
-1 |
-1.2 |
-1.2 |
-0.6 |
-0.9 |
-0.3 |
At2g45300 |
246627_s_at (m) |
|
3-phosphoshikimate 1-carboxyvinyltransferase / 5-enolpyruvylshikimate-3-phosphate / EPSP synthase |
10 |
glyphosate metabolism | aromatic amino acid family biosynthesis, shikimate pathway |
|
chorismate biosynthesis |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
2.90 |
4.89 |
At5g47730 |
0.639 |
|
SEC14 cytosolic factor, putative; similar to polyphosphoinositide binding protein SEC14 homolog Ssh1p (Glycine max) |
0.9 |
1.8 |
0.5 |
0.7 |
0.5 |
0.4 |
0.7 |
0.9 |
0.8 |
0.6 |
0.6 |
1.5 |
1.4 |
1.4 |
1.2 |
0.9 |
0.6 |
0.9 |
1.1 |
2 |
1.8 |
-0.6 |
0.1 |
-0.1 |
-0.8 |
-0.1 |
-0.3 |
-0.2 |
-0.1 |
-0.4 |
-0.3 |
-0.5 |
0.2 |
-0.3 |
0 |
-0.1 |
-0.3 |
-0.1 |
-0.6 |
-0.5 |
-0.2 |
0 |
0 |
0 |
-0.6 |
-0.3 |
-0.1 |
-0.1 |
-0.1 |
-0.9 |
-0.4 |
-0.5 |
0.4 |
-0.2 |
-0.3 |
-0.6 |
0.5 |
0.3 |
0.8 |
0.7 |
1.2 |
0.9 |
1.5 |
0.5 |
-0.3 |
0.2 |
0.2 |
-0.3 |
-0.3 |
-0.2 |
-0.5 |
-0.2 |
-0.4 |
-0.6 |
-0.2 |
0 |
-0.5 |
-0.6 |
0.1 |
-0.1 |
-0.2 |
-0.5 |
-0.4 |
0 |
-0.2 |
0 |
0 |
0 |
0 |
-0.4 |
-0.2 |
0.8 |
1.5 |
1.3 |
0.8 |
1.1 |
0.4 |
1.3 |
0 |
0.2 |
1.1 |
1 |
1.4 |
0.7 |
1.1 |
1.1 |
0 |
0.7 |
-0.3 |
-0.4 |
-0.3 |
0 |
-0.1 |
-0.2 |
-0.2 |
0 |
0 |
0 |
0 |
-0.1 |
0.1 |
0.2 |
0.2 |
0 |
0.3 |
0 |
0.4 |
0.1 |
0.3 |
0 |
0 |
-0.2 |
-0.1 |
0.7 |
1.2 |
-0.2 |
-0.5 |
-0.3 |
0.1 |
-0.1 |
-0.2 |
-1.4 |
-1.5 |
-1.1 |
-1.1 |
-1.1 |
0.4 |
0.2 |
0 |
0.3 |
-0.3 |
-0.6 |
-0.7 |
-1.2 |
-1.4 |
-1.5 |
-1.3 |
-1.7 |
-1.3 |
-1.6 |
-1.8 |
-2 |
-0.3 |
-0.3 |
-1.8 |
-1.8 |
-1.6 |
At5g47730 |
248769_at |
|
SEC14 cytosolic factor, putative; similar to polyphosphoinositide binding protein SEC14 homolog Ssh1p (Glycine max) |
4 |
|
|
|
|
|
Miscellaneous acyl lipid metabolism |
|
|
2.86 |
4.10 |
At1g61820 |
0.636 |
|
glycosyl hydrolase family 1 protein; similar to beta-mannosidase (Lycopersicon esculentum) |
1.9 |
2.4 |
0.1 |
0.3 |
-0.2 |
0.9 |
1.2 |
1.7 |
1.9 |
0.8 |
4.2 |
4.6 |
4.2 |
4.6 |
4.2 |
3.3 |
1.9 |
-0.7 |
0.3 |
2.6 |
4.3 |
5 |
5.1 |
-0.3 |
2.2 |
0.5 |
0.4 |
1.7 |
1.9 |
1.7 |
2.2 |
0.2 |
0.3 |
2.2 |
1.6 |
0.8 |
0.6 |
1.1 |
0.9 |
0.5 |
0.3 |
0.3 |
0.8 |
0.3 |
0.5 |
0.5 |
0.2 |
0 |
0.2 |
2.9 |
3.4 |
-2.4 |
3.3 |
2.2 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
0 |
0 |
3.8 |
0.2 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
0.9 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-0.9 |
-0.8 |
-0.1 |
-0.9 |
-2.4 |
3.5 |
-2.4 |
-2.4 |
3 |
2.7 |
3.7 |
3.2 |
0.3 |
-2.4 |
3.3 |
3.1 |
3.1 |
2.5 |
2.1 |
0.5 |
-1.1 |
2 |
1.2 |
-0.4 |
0 |
-0.1 |
0.6 |
1 |
0.6 |
0 |
-0.3 |
0.7 |
0.2 |
-0.6 |
-1.3 |
-1.6 |
-1.6 |
-0.2 |
0 |
-0.3 |
0.8 |
0 |
0.4 |
-0.7 |
-1.1 |
-2.4 |
-2.4 |
-0.5 |
-2.4 |
-2.4 |
-2.4 |
-0.7 |
-2.4 |
-2 |
-0.1 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
-2.4 |
1 |
-0.4 |
-0.2 |
0.1 |
0.3 |
0.6 |
0.9 |
1.2 |
1.8 |
1.6 |
-1.9 |
-2.4 |
-0.8 |
-2.4 |
-2.4 |
-2.4 |
0.5 |
0.5 |
-2.4 |
-2.4 |
-2.2 |
At1g61820 |
264280_at |
|
glycosyl hydrolase family 1 protein; similar to beta-mannosidase (Lycopersicon esculentum) |
1 |
|
|
|
|
|
|
|
Glycoside Hydrolase, Family 1 |
6.29 |
7.64 |
At2g37040 |
0.627 |
PAL1 |
phenylalanine ammonia-lyase 1 |
-3.8 |
2.1 |
-1.1 |
-3.8 |
-2.9 |
-3.8 |
-3.8 |
-3 |
-3.8 |
-3.8 |
0.4 |
2.2 |
1.5 |
1.4 |
0 |
-1 |
-3.8 |
-3.8 |
-2.8 |
-1 |
0.4 |
-0.9 |
3.2 |
1.1 |
0.6 |
1.1 |
-0.7 |
-0.8 |
0 |
-0.4 |
0 |
1.9 |
1.6 |
1.5 |
1.4 |
1.4 |
1.5 |
0.5 |
0.5 |
0.5 |
1.5 |
1.9 |
1.3 |
0.9 |
0.5 |
0.9 |
1.4 |
1.8 |
1.4 |
0.6 |
1.5 |
0.7 |
1.2 |
-0.7 |
0 |
-1.7 |
2.3 |
1.4 |
1 |
0.1 |
2.3 |
1 |
1.3 |
1.1 |
0.3 |
0.1 |
0.1 |
0.8 |
0.6 |
0.8 |
1 |
2 |
0.6 |
-0.2 |
-0.3 |
1.1 |
0.3 |
-1 |
0 |
0.3 |
0.6 |
0.5 |
0.5 |
0 |
-0.3 |
-0.7 |
0.2 |
0 |
-0.3 |
0 |
-1.1 |
1.4 |
0 |
-0.4 |
1.7 |
2.4 |
0.9 |
3.1 |
-0.8 |
-0.2 |
3 |
2.8 |
3 |
2.1 |
3.3 |
3.5 |
0.9 |
1.9 |
1.5 |
0.1 |
-0.4 |
-1.4 |
-1.7 |
-1.9 |
-1.9 |
-2.3 |
0 |
-1 |
-1.7 |
-1.6 |
0.4 |
0.9 |
1.3 |
0.9 |
1.3 |
1.6 |
1.1 |
0.7 |
0 |
0 |
1.1 |
-0.2 |
0.4 |
1.3 |
1.3 |
0.9 |
1.7 |
0 |
0.5 |
0.7 |
0.4 |
-3.8 |
-3.8 |
-3.8 |
-3.8 |
-3.8 |
2.7 |
0 |
0.5 |
1.9 |
1.4 |
0.4 |
1 |
-0.3 |
0.1 |
0 |
-3.8 |
-3.8 |
-1.1 |
-3.8 |
-3.8 |
-3.8 |
0 |
0 |
-3.8 |
-3.8 |
-4.2 |
At2g37040 |
263845_at |
PAL1 |
phenylalanine ammonia-lyase 1 |
10 |
defense response | response to wounding | phenylpropanoid biosynthesis | phenylalanine ammonia-lyase activity |
amino acid metabolism | metabolism of the cysteine - aromatic group | biosynthesis of secondary products derived from L-phenylalanine and L-tyrosine | biosynthesis of phenylpropanoids |
salicylic acid biosynthesis | suberin biosynthesis | lignin biosynthesis | phenylpropanoid pathway, initial reactions |
Nitrogen metabolism | Tyrosine metabolism | Phenylalanine metabolism | Alkaloid biosynthesis II |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
|
6.33 |
7.83 |
At4g34230 |
0.627 |
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. |
2 |
2.3 |
2.3 |
1.9 |
1.5 |
1.4 |
1.7 |
1.8 |
2 |
2.1 |
2.8 |
3.2 |
2.6 |
2.6 |
2.2 |
1.8 |
1.1 |
1.7 |
1.4 |
2.3 |
2.6 |
2.3 |
3.2 |
-0.5 |
-1.8 |
0.6 |
0.7 |
1.2 |
1.2 |
0.6 |
0.3 |
-0.3 |
1.1 |
0 |
-0.4 |
0.8 |
0.8 |
0.2 |
0.1 |
0 |
0.5 |
0.4 |
0.6 |
0.2 |
0.1 |
0.3 |
0.3 |
0.4 |
0.9 |
-0.5 |
0 |
-0.8 |
0.4 |
1.6 |
-0.7 |
-0.7 |
1.9 |
1.7 |
2.1 |
0.4 |
1.9 |
1.7 |
2.6 |
1.7 |
-1.6 |
-1.7 |
-0.3 |
0.1 |
-0.9 |
-1.2 |
-0.9 |
-0.4 |
-0.2 |
-0.5 |
-0.9 |
0.5 |
-0.8 |
-0.8 |
-0.9 |
-0.9 |
-1 |
-1.3 |
-1.2 |
-0.9 |
-1.6 |
-1.3 |
-0.1 |
0.5 |
0.6 |
1.8 |
0 |
0.2 |
-0.1 |
0 |
0.8 |
1 |
1.2 |
0.5 |
-0.1 |
-0.9 |
2 |
1.8 |
0.7 |
1.1 |
2.7 |
2.9 |
-0.1 |
1.4 |
2.9 |
-1.9 |
-1.7 |
-1.8 |
-2.6 |
-2.5 |
-2.3 |
-2.7 |
-1.8 |
-1.4 |
-2 |
-1.9 |
-0.2 |
-0.1 |
0.6 |
0.4 |
0.4 |
-0.4 |
-0.3 |
0.9 |
0.8 |
-0.5 |
0 |
-0.6 |
1 |
1.7 |
0.5 |
0.5 |
1.4 |
1.2 |
-0.9 |
-0.5 |
-0.9 |
-4.4 |
-4.4 |
-4.4 |
-1.7 |
-0.4 |
1 |
0.5 |
-0.4 |
1.5 |
1 |
-0.3 |
-0.1 |
-1 |
-1.8 |
-1.5 |
-4.4 |
-4.4 |
-3.3 |
-3.8 |
-4.4 |
-4.4 |
-0.7 |
-0.7 |
-4.4 |
-4.4 |
-4.4 |
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 |
|
7.05 |
7.68 |
At1g62790 |
0.624 |
|
protease inhibitor/seed storage/lipid transfer protein (LTP) family protein |
1 |
0.6 |
0.3 |
0 |
-0.5 |
-0.5 |
-0.4 |
-0.4 |
-0.2 |
-0.6 |
0.1 |
1.2 |
1 |
0.7 |
0.2 |
-0.2 |
-0.5 |
-0.8 |
-0.2 |
0.7 |
1.4 |
1.5 |
2.1 |
-0.7 |
-1.3 |
1.2 |
0.7 |
1.3 |
1.3 |
1.2 |
1.3 |
-0.5 |
0.7 |
-0.6 |
0.4 |
0.9 |
-0.3 |
-0.2 |
-0.7 |
-0.3 |
-0.2 |
-0.5 |
-0.5 |
-0.7 |
-0.6 |
-0.3 |
-0.2 |
-0.4 |
-0.2 |
0.1 |
-0.7 |
-0.6 |
1.6 |
1.5 |
-2.3 |
-1.5 |
1.8 |
1.2 |
-0.4 |
-0.8 |
0.4 |
1.9 |
2.7 |
2.1 |
-0.6 |
-0.6 |
-0.1 |
0 |
-0.3 |
-1.3 |
-1.1 |
-1 |
-0.8 |
-0.5 |
-0.9 |
0.4 |
-0.6 |
-0.7 |
-0.5 |
0.1 |
-0.5 |
-2.1 |
-2.1 |
0 |
-0.5 |
-0.4 |
-0.2 |
-0.4 |
0 |
-0.6 |
-1.2 |
1.6 |
0.1 |
0.3 |
1.7 |
1.8 |
1.2 |
2.1 |
-1 |
-1.1 |
2.1 |
1.8 |
2.1 |
1.2 |
0.6 |
0 |
-0.5 |
0.8 |
-0.9 |
-0.5 |
0.2 |
0.4 |
1 |
1 |
0.7 |
1 |
1.2 |
1.1 |
1.1 |
1.1 |
0 |
-0.3 |
-0.7 |
-0.2 |
-0.3 |
0 |
0.3 |
-0.9 |
-0.5 |
0 |
0 |
-0.4 |
-0.8 |
-0.2 |
-0.8 |
0 |
-1.5 |
-0.2 |
-1 |
0 |
-0.1 |
-0.6 |
-1.2 |
-2.1 |
-2.1 |
-2.1 |
0.9 |
0.5 |
0.8 |
1.1 |
1.2 |
1.4 |
1.5 |
1 |
0.5 |
0.3 |
-2.2 |
-1.9 |
-0.6 |
-1.3 |
-1.6 |
0.4 |
-0.2 |
-0.2 |
-1.9 |
-1.6 |
-0.9 |
At1g62790 |
262694_at |
|
protease inhibitor/seed storage/lipid transfer protein (LTP) family protein |
2 |
|
|
|
|
|
Miscellaneous acyl lipid metabolism |
|
|
3.68 |
5.16 |
At1g06550 |
0.619 |
|
Enoyl-CoA hydratase/isomerase family protein |
-0.9 |
1.5 |
0.9 |
-0.2 |
-0.6 |
-1 |
-0.8 |
-0.5 |
-0.3 |
-1.1 |
0.7 |
2.7 |
2.9 |
2.2 |
1.1 |
-0.1 |
-1.1 |
-1.3 |
-0.1 |
0.8 |
1.5 |
-1.4 |
1 |
0.4 |
0 |
1.8 |
0.6 |
0.9 |
1.6 |
1.1 |
1.6 |
0.1 |
0.3 |
0.2 |
-0.1 |
0 |
0.2 |
-0.3 |
-0.2 |
-0.5 |
0.6 |
0.6 |
0 |
-0.5 |
-0.5 |
-0.3 |
0.3 |
0.8 |
0.3 |
-1.8 |
-1.3 |
-0.8 |
0.7 |
-0.6 |
-1.6 |
-2 |
1 |
-0.4 |
-1.8 |
-2.1 |
-0.5 |
-0.1 |
1.1 |
1.7 |
-0.4 |
-0.4 |
-0.8 |
-0.6 |
-0.3 |
-0.8 |
-1.1 |
-0.2 |
-0.8 |
-1.3 |
-0.5 |
0.2 |
0.2 |
-0.5 |
0 |
0.3 |
0.4 |
-0.4 |
-0.6 |
-0.5 |
-0.8 |
-1 |
-1.2 |
-1.5 |
-1.8 |
-1.4 |
-1.5 |
0.8 |
-2.1 |
-2.1 |
0.6 |
1 |
0.1 |
2.4 |
-0.6 |
-0.3 |
2.1 |
2 |
2.3 |
1 |
2.2 |
1.9 |
0.3 |
1.7 |
0.7 |
0.6 |
0.6 |
1.2 |
0.6 |
0.6 |
0.8 |
0.9 |
1 |
1 |
1.1 |
1.3 |
1.3 |
1.5 |
1.6 |
0.8 |
1.1 |
1.1 |
1.6 |
0 |
0.3 |
0.7 |
1.5 |
-0.2 |
-0.4 |
-1 |
2.2 |
0.3 |
0.6 |
0 |
1.6 |
1.4 |
0.6 |
-0.3 |
-0.1 |
-2.1 |
-2.1 |
-2.1 |
1.2 |
-2.1 |
1.8 |
1.1 |
0.2 |
0.1 |
0.1 |
-0.6 |
-1.8 |
-2 |
-2.1 |
-2.1 |
-1.3 |
-1.7 |
-2.1 |
-2.1 |
-1.7 |
-1.7 |
-2.1 |
-2.1 |
-2.1 |
At1g06550 |
262619_at |
|
Enoyl-CoA hydratase/isomerase family protein |
2 |
|
|
valine degradation II | valine degradation I |
|
|
|
|
|
4.14 |
5.05 |
At5g54160 |
0.619 |
ATOMT1 |
A caffeic acid/5-hydroxyferulic acid O-methyltransferase. Interacts with 14-4-3 proteins in yeast 2 hybrid assay. |
-1.1 |
0.3 |
1.5 |
0.7 |
-0.1 |
-0.8 |
-1 |
-0.7 |
-0.5 |
-1 |
0.9 |
2 |
2 |
1.9 |
1.3 |
0.5 |
0 |
-1 |
-0.8 |
-0.1 |
0.9 |
-0.9 |
0.8 |
1.1 |
0.2 |
0.1 |
-0.2 |
0 |
0.2 |
-0.6 |
-0.3 |
0.1 |
0.4 |
0.9 |
0.4 |
1 |
0.3 |
0.4 |
-0.3 |
-0.1 |
0 |
0.2 |
0.3 |
0.1 |
-0.2 |
0 |
-0.1 |
0.1 |
0.4 |
0.6 |
0.9 |
0.7 |
1 |
0 |
0.3 |
-0.6 |
1.2 |
0.8 |
0.3 |
0.1 |
1.4 |
1 |
0.7 |
1 |
-1.2 |
-1.7 |
-0.7 |
-0.1 |
-0.9 |
-0.9 |
-0.8 |
-0.1 |
0.2 |
-0.3 |
-1.2 |
0.3 |
0.3 |
-0.2 |
-0.9 |
-1 |
-0.8 |
-0.7 |
-0.6 |
-0.7 |
-0.7 |
-0.7 |
-1 |
0.2 |
0.7 |
0 |
-1.6 |
0.6 |
2 |
1.8 |
1.5 |
1.4 |
1 |
2 |
-0.2 |
-0.4 |
1.6 |
1.5 |
2 |
1.9 |
2.4 |
2.7 |
0.1 |
1.3 |
1.3 |
-0.1 |
-0.2 |
-0.7 |
-0.4 |
-0.3 |
-0.7 |
-0.6 |
-0.2 |
-0.3 |
-0.6 |
-0.5 |
1 |
1.1 |
0.9 |
0.3 |
1 |
0.8 |
-0.4 |
0.2 |
0.4 |
0.1 |
0.9 |
-0.7 |
0.1 |
0.2 |
1.5 |
0.3 |
0.9 |
0.4 |
0 |
-0.2 |
-1.6 |
-1 |
0.4 |
0 |
-0.4 |
-4.2 |
0.7 |
-0.7 |
-1.2 |
1.3 |
1.1 |
0.9 |
1.1 |
0.7 |
0.4 |
0 |
-4.2 |
-4.2 |
-3 |
-2.6 |
-4.2 |
-4.2 |
-0.8 |
-0.8 |
-2.6 |
-2.7 |
-0.9 |
At5g54160 |
248200_at |
ATOMT1 |
A caffeic acid/5-hydroxyferulic acid O-methyltransferase. Interacts with 14-4-3 proteins in yeast 2 hybrid assay. |
10 |
lignin biosynthesis | caffeate O-methyltransferase activity |
|
suberin biosynthesis | lignin biosynthesis | phenylpropanoid biosynthesis |
Flavonoid biosynthesis |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
Methyltransferase, COMT like |
4.29 |
7.06 |
At2g22250 |
0.617 |
|
aminotransferase class I and II family protein, similar to aspartate aminotransferase from Bacillus stearothermophilus and Thermus aquaticu |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
1.1 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
1.7 |
0.4 |
0.3 |
0.2 |
0.2 |
0.8 |
-0.9 |
-1.6 |
-1.1 |
-0.6 |
1.2 |
0.4 |
1.6 |
1.2 |
1.4 |
1.9 |
1.8 |
1.2 |
1.5 |
1.4 |
1.3 |
1.9 |
2 |
1.6 |
1.6 |
1.5 |
1.5 |
1.6 |
0 |
0.1 |
1.6 |
3.6 |
1.5 |
1.1 |
1.8 |
0.4 |
-0.2 |
2.5 |
2.1 |
-0.2 |
0 |
-0.3 |
-0.2 |
0.7 |
0.8 |
1.2 |
1.2 |
1.4 |
1.6 |
1.1 |
0.8 |
0.9 |
0.7 |
0.7 |
1.9 |
1 |
0.7 |
1.4 |
1.4 |
1.7 |
0.6 |
1 |
2 |
1 |
1.3 |
3 |
0 |
0 |
-0.7 |
1.3 |
3.2 |
1.7 |
0.2 |
0.9 |
1.8 |
1.5 |
0 |
-1.6 |
-1.6 |
2.7 |
2.8 |
0.5 |
-0.7 |
0.8 |
-1.2 |
-1.6 |
0.3 |
0 |
0.3 |
0.6 |
-0.1 |
0.9 |
1.2 |
1.1 |
0.1 |
1.5 |
1.7 |
0.7 |
0.7 |
-1.6 |
-1.3 |
-0.3 |
-0.3 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-0.8 |
-1.6 |
-0.8 |
-1.6 |
-0.4 |
0 |
-1.6 |
-1.1 |
-1.6 |
-1.6 |
0 |
-0.7 |
-1.1 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
0.1 |
-1.6 |
-1.6 |
1 |
1 |
-1.6 |
-1.6 |
-0.4 |
At2g22250 |
263429_at |
|
aminotransferase class I and II family protein, similar to aspartate aminotransferase from Bacillus stearothermophilus and Thermus aquaticu |
2 |
|
|
asparagine biosynthesis I | aspartate biosynthesis and degradation | histidine biosynthesis I | phenylalanine biosynthesis II | asparagine degradation I | aspartate degradation I | aspartate degradation II | glutamine degradation III | phenylalanine degradation I | tyrosine degradation |
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 |
|
|
|
|
3.65 |
5.30 |
At1g02500 |
0.613 |
SAM1 |
S-adenosylmethionine synthetase gene sam-1 |
-0.6 |
0.3 |
0 |
-0.7 |
-0.4 |
-0.6 |
-0.3 |
-0.6 |
-0.6 |
-0.3 |
-0.3 |
1.4 |
1.2 |
0.9 |
0.4 |
0.1 |
-0.3 |
0 |
-0.5 |
0 |
-0.1 |
-1.3 |
-0.3 |
0.4 |
0 |
1.1 |
0.9 |
0.9 |
0.9 |
0.7 |
0.8 |
0.8 |
0.6 |
0.4 |
0.5 |
0.7 |
0.4 |
0.4 |
0.2 |
0.4 |
0.5 |
0.4 |
0.5 |
0.3 |
0.6 |
0.5 |
0.5 |
0.4 |
0.5 |
0.8 |
0.5 |
0.1 |
0.4 |
0.8 |
0.3 |
0.1 |
0.9 |
1.2 |
0.1 |
0.2 |
1.3 |
1 |
1.5 |
1.4 |
-0.3 |
-0.5 |
-0.3 |
0 |
0.1 |
0.3 |
0.1 |
0 |
-0.1 |
-0.4 |
-0.3 |
0.4 |
-0.2 |
-0.5 |
-0.3 |
-0.1 |
0.1 |
-0.1 |
-0.1 |
-0.1 |
-0.2 |
-0.1 |
0.5 |
-0.7 |
-0.9 |
0 |
0.6 |
1 |
0 |
-0.6 |
1.4 |
1.2 |
0.5 |
1.4 |
-0.4 |
-0.2 |
1 |
1.2 |
1.3 |
0.7 |
2.2 |
2.2 |
0 |
1.3 |
0.9 |
0.2 |
0.2 |
0 |
-0.3 |
-0.1 |
-0.2 |
-0.2 |
-0.3 |
-0.4 |
-0.4 |
-0.2 |
0.1 |
0 |
0.3 |
0 |
0.3 |
0.3 |
0.5 |
-0.1 |
-0.1 |
-0.8 |
0 |
-0.3 |
0 |
0.4 |
0.2 |
-0.3 |
0.6 |
-0.2 |
0.1 |
0.3 |
0.5 |
-1.7 |
-1.5 |
-1.3 |
-1.4 |
-0.7 |
1.3 |
-0.1 |
-0.2 |
1.3 |
0.9 |
0.2 |
0.4 |
0.2 |
0 |
-0.1 |
-4.4 |
-4.3 |
-2.6 |
-2.5 |
-4.5 |
-3.4 |
-0.3 |
-0.3 |
-3.9 |
-4.2 |
-1.9 |
At1g02500 |
260913_at |
SAM1 |
S-adenosylmethionine synthetase gene sam-1 |
10 |
ethylene biosynthesis |
|
methionine and S-adenosylmethionine synthesis | methionine degradation I |
Methionine metabolism | Selenoamino acid metabolism |
Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate |
|
|
|
3.27 |
6.78 |
At3g18280 |
0.610 |
|
protease inhibitor/seed storage/lipid transfer protein (LTP) family protein, similar to TED4 (Zinnia elegans) |
2.5 |
2.2 |
2.3 |
2.3 |
2.4 |
2.3 |
1.9 |
1.2 |
1.5 |
1.6 |
-3.5 |
0.7 |
1.7 |
1.6 |
1.8 |
2.7 |
2.9 |
1.7 |
1.7 |
1.3 |
-0.1 |
-0.4 |
-0.8 |
0.9 |
-1.2 |
3 |
2.9 |
2.9 |
2.6 |
2 |
1.8 |
0.3 |
0.8 |
0.4 |
0.3 |
1.6 |
1.6 |
1.7 |
1.4 |
1 |
1.2 |
1.1 |
1.4 |
1.2 |
1.3 |
1.4 |
1.1 |
1.3 |
1.6 |
0 |
0.2 |
0 |
1.6 |
0.3 |
-0.6 |
-1.6 |
0.4 |
-0.2 |
-1.5 |
-1.5 |
0.6 |
2.5 |
2.3 |
4.1 |
-0.8 |
-1.3 |
-0.8 |
-0.6 |
-1.1 |
-0.9 |
-0.6 |
-0.8 |
-0.6 |
-0.8 |
-1 |
1.9 |
1.1 |
0.9 |
1.1 |
1.2 |
1 |
-0.2 |
-0.4 |
1.2 |
0.4 |
0.1 |
0 |
-0.4 |
-0.1 |
-2.8 |
-0.1 |
2.4 |
1 |
1.9 |
2.1 |
2.4 |
3.1 |
2.5 |
-0.6 |
0 |
1.8 |
2.1 |
2.6 |
1.6 |
1.7 |
1.9 |
-0.1 |
2.7 |
2.5 |
-0.4 |
-0.2 |
-1.1 |
0.7 |
0.2 |
-0.2 |
-1 |
0.8 |
1 |
0.1 |
-0.4 |
-1.2 |
-1.7 |
-1.4 |
-0.6 |
-0.6 |
0.8 |
0.7 |
-0.6 |
-0.9 |
-0.3 |
-1.2 |
0.3 |
-1.6 |
-2.4 |
-2.1 |
-3.6 |
-3.5 |
-3.5 |
-1.6 |
-0.9 |
0.2 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-2.9 |
-2.8 |
0.7 |
-0.9 |
-1.9 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-3.5 |
-2.2 |
-3.5 |
-3.5 |
-2.6 |
-2.6 |
-3.5 |
-3.5 |
-1.2 |
At3g18280 |
257066_at |
|
protease inhibitor/seed storage/lipid transfer protein (LTP) family protein, similar to TED4 (Zinnia elegans) |
2 |
|
|
|
|
|
Miscellaneous acyl lipid metabolism |
|
|
6.18 |
7.76 |
At5g49720 |
0.607 |
KOR1 |
endo-1,4-beta-glucanase KORRIGAN (KOR) / cellulase (OR16pep), Encodes a cell plate localized endo-1,4-beta-glucanase. Is essential for cytokinesis. |
0.3 |
-0.5 |
0 |
0 |
0 |
-0.1 |
0 |
0 |
-0.2 |
0 |
0.4 |
0.1 |
0.3 |
0 |
0 |
0 |
-0.1 |
-0.3 |
0.2 |
0.5 |
0.9 |
0.6 |
-0.4 |
0.2 |
1 |
0.4 |
0.5 |
0.9 |
0.8 |
0.8 |
0.7 |
0.5 |
0.6 |
0.6 |
0.4 |
0.6 |
0.4 |
0.5 |
0.2 |
0.4 |
0.4 |
0.2 |
0.1 |
0.3 |
0.1 |
0.3 |
0.2 |
0 |
0.2 |
0.1 |
1 |
0.3 |
0.6 |
0.3 |
0.6 |
0.4 |
0.5 |
0.3 |
0.4 |
0.3 |
0.2 |
0.1 |
0.2 |
0.5 |
-0.1 |
0.1 |
0.3 |
0.5 |
0.6 |
0.6 |
0.7 |
0.5 |
0.1 |
0 |
-0.1 |
0.3 |
-0.3 |
-0.4 |
-0.3 |
0 |
0.2 |
0 |
-0.1 |
0.7 |
0.7 |
0.8 |
0.3 |
-0.4 |
-0.5 |
-0.1 |
0.5 |
0.5 |
0.2 |
-0.4 |
0.5 |
0.5 |
0.5 |
1.1 |
-0.2 |
-0.2 |
0.1 |
0.2 |
1 |
1.9 |
2.3 |
1.7 |
0.1 |
1.6 |
0.4 |
-0.1 |
-0.4 |
-0.6 |
-0.2 |
-0.2 |
-0.4 |
-0.3 |
0 |
-0.1 |
-0.3 |
-0.2 |
-0.5 |
-0.1 |
-0.1 |
-0.1 |
0.1 |
0 |
0.4 |
-0.4 |
-0.4 |
0 |
-0.5 |
0 |
-0.8 |
-0.7 |
0.2 |
0.3 |
-0.4 |
-0.1 |
-0.1 |
-0.1 |
0.5 |
-3.3 |
-2.1 |
-3.7 |
-3.5 |
-4 |
0.5 |
0.3 |
-0.1 |
0.7 |
0.4 |
-0.3 |
-0.1 |
-1 |
-1.3 |
-1.4 |
-2 |
-2.2 |
-1.5 |
-0.7 |
-2.2 |
-1.5 |
0.4 |
0.4 |
-0.8 |
-1 |
-0.2 |
At5g49720 |
248573_at |
KOR1 |
endo-1,4-beta-glucanase KORRIGAN (KOR) / cellulase (OR16pep), Encodes a cell plate localized endo-1,4-beta-glucanase. Is essential for cytokinesis. |
4 |
unidimensional cell growth | cellulose biosynthesis |
|
cellulose biosynthesis |
|
|
|
|
|
2.49 |
6.38 |
At3g03050 |
0.601 |
CSLD3 |
encodes a cellulose synthase like protein. mutations initiate root hairs that rupture at their tip soon after initiation. is required for the synthesis of a noncellulosic wall polysaccharide. |
0.8 |
-0.3 |
0.4 |
0.9 |
0.6 |
0.7 |
1.1 |
0.9 |
0.9 |
0.9 |
0.1 |
1.2 |
1.2 |
1.5 |
1.5 |
1.7 |
1.4 |
0.9 |
1.1 |
1.1 |
2.2 |
0.5 |
0.8 |
-0.1 |
-0.5 |
1 |
0.3 |
0.5 |
0.5 |
0.5 |
0.9 |
0 |
0.2 |
-0.5 |
0.3 |
0.5 |
0.2 |
0.1 |
0.2 |
0.3 |
0.4 |
0.2 |
0 |
-0.2 |
0.1 |
0.3 |
0.1 |
0.2 |
-0.3 |
0.1 |
0.1 |
-0.4 |
0.4 |
-1 |
-1.1 |
-0.1 |
0.1 |
0 |
1.5 |
1.1 |
-0.1 |
-0.2 |
0 |
0.3 |
-0.8 |
-0.5 |
-0.1 |
-0.4 |
-0.3 |
-0.8 |
0 |
-0.5 |
-0.9 |
-0.7 |
-0.9 |
-0.2 |
-0.7 |
-0.6 |
-0.5 |
-0.5 |
-1 |
-0.7 |
-0.7 |
-0.4 |
-0.4 |
-0.2 |
0.4 |
-1 |
-1.1 |
-0.8 |
-0.5 |
1.3 |
0.5 |
0.6 |
0.5 |
1.4 |
0.6 |
2.5 |
-0.5 |
-0.5 |
2.5 |
2.3 |
2.2 |
1.1 |
-0.6 |
-0.8 |
0 |
0.2 |
-0.5 |
-0.1 |
-0.2 |
-0.2 |
-0.3 |
-0.2 |
-0.1 |
0 |
0.2 |
0.1 |
0.2 |
0.3 |
-0.3 |
-0.4 |
-0.4 |
-0.8 |
0.1 |
0.1 |
0.4 |
-0.2 |
-0.1 |
0.1 |
-0.5 |
0.3 |
-0.6 |
-0.7 |
0 |
-0.7 |
-0.9 |
-0.8 |
-0.1 |
-0.4 |
-0.6 |
-1.3 |
-1.7 |
-1.3 |
-1.3 |
-1.3 |
-0.4 |
-0.6 |
-0.4 |
0 |
0 |
0.1 |
-0.4 |
-0.9 |
-1.2 |
-1.1 |
-1.6 |
-1.5 |
-0.6 |
0.2 |
-1.8 |
-1.5 |
0.4 |
0.4 |
-0.2 |
-0.7 |
0 |
At3g03050 |
258850_at |
CSLD3 |
encodes a cellulose synthase like protein. mutations initiate root hairs that rupture at their tip soon after initiation. is required for the synthesis of a noncellulosic wall polysaccharide. |
10 |
|
|
cellulose biosynthesis |
|
Cell Wall Carbohydrate Metabolism | cellulose biosynthesis |
|
|
|
2.84 |
4.37 |
At3g21240 |
0.599 |
4CL2 |
encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it does NOT convert ferulate. |
-0.9 |
-0.3 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
0 |
2.5 |
1.7 |
1.3 |
0.3 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
1.3 |
0.3 |
-1.7 |
1 |
-0.1 |
-0.9 |
0.7 |
0.3 |
0.2 |
0.7 |
1.3 |
0 |
0.5 |
0.6 |
0.9 |
0.6 |
0.7 |
0.7 |
0.8 |
0.9 |
1 |
1 |
1 |
0.7 |
1 |
1.1 |
0.8 |
-0.9 |
-0.5 |
-1.1 |
1.7 |
0.1 |
-0.8 |
-0.9 |
-0.3 |
-0.6 |
-0.9 |
-0.9 |
1.7 |
1.1 |
2.7 |
2.3 |
-1 |
-0.9 |
-0.6 |
-0.8 |
-0.9 |
-0.6 |
-0.9 |
-0.7 |
-0.9 |
-0.9 |
-0.9 |
0.4 |
-0.9 |
-0.9 |
-0.6 |
-0.3 |
-0.3 |
-0.7 |
-0.2 |
-0.1 |
-1.4 |
-0.9 |
-0.5 |
-0.2 |
-0.1 |
-0.8 |
-1.2 |
1.9 |
0.4 |
-0.9 |
1.9 |
2.7 |
1.5 |
3 |
-0.9 |
-0.2 |
2.2 |
2.2 |
3 |
-0.2 |
1.5 |
2.7 |
0.1 |
0.2 |
1.1 |
-1.1 |
-0.1 |
-0.9 |
-0.8 |
-0.6 |
-0.5 |
-0.7 |
0.3 |
0.4 |
0.1 |
0 |
-0.8 |
-0.7 |
1 |
0 |
0.7 |
-0.5 |
-0.4 |
0.3 |
0.3 |
-0.2 |
-0.4 |
-0.4 |
-1.6 |
-0.8 |
-0.7 |
-1.3 |
2.3 |
-0.4 |
-0.9 |
-0.1 |
-1 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
1.3 |
1 |
-0.4 |
1 |
0.9 |
1.4 |
1.8 |
1.1 |
1 |
0.4 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
0 |
0 |
-0.9 |
-0.9 |
-0.9 |
At3g21240 |
258047_at |
4CL2 |
encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. In addition to 4-coumarate, it does NOT convert ferulate. |
10 |
4-coumarate-CoA ligase activity | response to UV | response to pathogenic fungi | response to wounding | phenylpropanoid metabolism |
|
suberin biosynthesis | lignin biosynthesis | flavonoid biosynthesis |
Stilbene, coumarine and lignin biosynthesis |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase |
3.24 |
4.74 |
At3g53260 |
0.587 |
PAL2 |
phenylalanine ammonia-lyase 2 |
-2.2 |
2.4 |
-1.4 |
-2.1 |
-2.2 |
-2.2 |
-2.2 |
-1.8 |
-2.2 |
-2.2 |
-0.7 |
3.2 |
2.5 |
2.5 |
1.1 |
-0.2 |
-1.5 |
-2.2 |
-2.2 |
-1 |
-0.5 |
-1.9 |
3.4 |
1.8 |
1.9 |
1 |
-1.2 |
-0.9 |
0 |
-0.1 |
0 |
2.5 |
1.1 |
2.2 |
0.1 |
0.7 |
1.8 |
1.5 |
0.6 |
1 |
1.5 |
1.7 |
1.6 |
1.5 |
1 |
0.7 |
1.5 |
1.5 |
1.7 |
1.1 |
1.5 |
1 |
0.2 |
-2.2 |
1.1 |
0.3 |
1.9 |
1 |
1.9 |
1.7 |
1 |
0.7 |
1.3 |
1 |
0 |
0 |
0.6 |
0.4 |
0.7 |
1.8 |
1.6 |
1.9 |
0.8 |
-0.2 |
-0.9 |
2 |
0.6 |
-0.5 |
0 |
0.4 |
1.3 |
-0.9 |
-0.3 |
0.3 |
0 |
-0.1 |
-0.3 |
-0.3 |
-0.4 |
0 |
-0.4 |
1 |
0.9 |
-1.1 |
0.7 |
1.1 |
1.3 |
2.5 |
-0.9 |
-1.1 |
2.4 |
2.2 |
2.3 |
1.8 |
2.2 |
1.8 |
-1.8 |
1.3 |
0.1 |
0.5 |
0 |
-0.7 |
-0.6 |
-0.5 |
-0.8 |
-0.7 |
-2.4 |
-3.1 |
-2.8 |
-3.3 |
0.6 |
0.6 |
0.5 |
0.1 |
-0.5 |
-0.1 |
-0.2 |
-1.6 |
-1.9 |
-0.3 |
0.6 |
-2.2 |
-0.5 |
-0.2 |
0.6 |
0.5 |
-0.1 |
0.3 |
-0.1 |
0 |
0.6 |
-2.2 |
-2.2 |
-2.2 |
-2.2 |
-2.2 |
1.2 |
-0.5 |
0.3 |
1.2 |
0.9 |
1.3 |
1 |
-0.1 |
-0.2 |
-0.7 |
-2.9 |
-2.7 |
-1.7 |
-2.2 |
-2.4 |
-3.4 |
-2.5 |
-2.5 |
-2.2 |
-2.2 |
-2.2 |
At3g53260 |
251984_at |
PAL2 |
phenylalanine ammonia-lyase 2 |
10 |
defense response | response to wounding | phenylpropanoid biosynthesis | phenylalanine ammonia-lyase activity |
amino acid metabolism | metabolism of the cysteine - aromatic group | biosynthesis of secondary products derived from L-phenylalanine and L-tyrosine | biosynthesis of phenylpropanoids |
salicylic acid biosynthesis | suberin biosynthesis | lignin biosynthesis | phenylpropanoid pathway, initial reactions |
Nitrogen metabolism | Tyrosine metabolism | Phenylalanine metabolism | Alkaloid biosynthesis II |
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
|
4.79 |
6.93 |
At5g61840 |
0.587 |
|
exostosin family protein |
0.5 |
0.4 |
0.5 |
0.5 |
0.3 |
0.4 |
0.6 |
0.5 |
0.2 |
0.2 |
0.1 |
0.5 |
0.3 |
0.1 |
0.1 |
0.3 |
0.3 |
0.3 |
0 |
0.4 |
0.3 |
0.3 |
0 |
-0.3 |
-0.4 |
0.2 |
0.3 |
0 |
-0.2 |
0 |
-0.2 |
-0.2 |
0.1 |
-0.4 |
0 |
-0.1 |
-0.1 |
0.1 |
-0.2 |
-0.2 |
-0.1 |
-0.1 |
-0.1 |
0.1 |
-0.2 |
-0.1 |
0 |
0 |
-0.2 |
0 |
-0.3 |
-0.3 |
0.2 |
-0.6 |
-0.1 |
0 |
0.2 |
0 |
0.2 |
0.1 |
0.3 |
0.1 |
0.1 |
0.1 |
-0.1 |
-0.3 |
0.1 |
-0.1 |
-0.2 |
-0.2 |
-0.3 |
-0.4 |
-0.5 |
-0.4 |
-0.3 |
-0.3 |
-0.6 |
-0.5 |
-0.3 |
-0.2 |
-0.4 |
-0.3 |
-0.4 |
-0.1 |
-0.4 |
-0.1 |
0 |
-0.5 |
-0.8 |
-0.3 |
-0.2 |
0.6 |
0.3 |
1 |
0.4 |
0.3 |
0.5 |
0.6 |
0.3 |
0.1 |
0.7 |
0.6 |
0.5 |
0.5 |
0.7 |
0.6 |
0.4 |
0.5 |
0 |
0 |
0.1 |
0.4 |
0.1 |
0.1 |
0.2 |
0.4 |
0 |
0.4 |
0.4 |
0.5 |
0.2 |
0 |
0.1 |
-0.3 |
0 |
-0.3 |
0.1 |
0.1 |
0 |
-0.1 |
0.1 |
0 |
-0.3 |
-0.5 |
0.2 |
-0.5 |
-0.3 |
-0.6 |
0.3 |
0.1 |
0 |
-0.3 |
-0.8 |
-0.7 |
-0.7 |
-0.7 |
0.3 |
-0.1 |
0.1 |
0.5 |
0.4 |
0.4 |
0.1 |
-0.3 |
-0.5 |
-0.4 |
-0.5 |
-0.9 |
-0.2 |
0 |
-1 |
-0.2 |
-0.1 |
-0.1 |
-0.2 |
-0.3 |
0 |
At5g61840 |
247496_at |
|
exostosin family protein |
10 |
|
|
|
|
Cell Wall Carbohydrate Metabolism | pectin metabolism |
|
|
|
1.18 |
2.05 |
At2g01140 |
0.584 |
|
fructose-bisphosphate aldolase, putative, similar to plastidic aldolase from Nicotiana paniculata |
0.9 |
0.9 |
1.4 |
1.3 |
1.2 |
1.2 |
1.2 |
1.1 |
1.2 |
1.1 |
0.2 |
1.4 |
1.8 |
1.9 |
1.5 |
1.4 |
1.3 |
0.6 |
1.2 |
0.7 |
1 |
0.6 |
1.7 |
0 |
-1.2 |
1.4 |
1.3 |
1.2 |
1.1 |
1 |
1 |
0 |
0 |
-0.5 |
-0.4 |
0.6 |
0 |
-0.1 |
-0.4 |
-0.1 |
0 |
-0.1 |
0 |
-0.1 |
0.1 |
-0.2 |
-0.2 |
-0.1 |
0 |
-0.3 |
-0.7 |
-0.6 |
0.4 |
-0.3 |
-0.9 |
-0.4 |
0.6 |
0.4 |
-0.2 |
-0.5 |
0.8 |
1.2 |
1.1 |
1.8 |
-1.3 |
-1.3 |
-1.2 |
-1 |
-0.9 |
-1 |
-1 |
-1.1 |
-1.3 |
-1.2 |
-1.3 |
0 |
-1.1 |
-1.3 |
-1 |
-0.9 |
-0.6 |
-1 |
-1.2 |
-0.6 |
-1.1 |
-1.1 |
-0.4 |
-1.5 |
-1.5 |
-0.6 |
-1 |
0.6 |
-0.7 |
-0.9 |
0.8 |
0.6 |
0.3 |
1.4 |
-0.9 |
-1.1 |
0.5 |
1 |
1.4 |
-1.2 |
-0.1 |
-0.3 |
-0.1 |
0.2 |
-0.5 |
-0.2 |
0.2 |
0.3 |
0.4 |
0.4 |
0.2 |
0.2 |
0.2 |
0.3 |
0.5 |
0.3 |
0.5 |
0.1 |
0.1 |
-0.5 |
0.3 |
0.1 |
0.2 |
0 |
0.1 |
-1.1 |
0.3 |
0 |
-0.6 |
-0.4 |
1 |
-1 |
0.1 |
-0.8 |
-0.2 |
-0.1 |
-0.6 |
0 |
0 |
-2.2 |
-2.3 |
-2.4 |
0 |
-0.1 |
-0.4 |
0.7 |
1.1 |
1.4 |
1.1 |
-0.8 |
-1.1 |
-1 |
-0.9 |
-0.5 |
0 |
-0.1 |
-0.6 |
-0.6 |
0.2 |
0.2 |
0.1 |
0.2 |
0.5 |
At2g01140 |
265735_at |
|
fructose-bisphosphate aldolase, putative, similar to plastidic aldolase from Nicotiana paniculata |
4 |
pentose-phosphate shunt |
C-compound and carbohydrate metabolism | glycolysis and gluconeogenesis | photosynthesis |
Calvin cycle | mannitol degradation | sorbitol fermentation | sorbitol degradation | fructose degradation (anaerobic) | acetate fermentation | glycolysis I | glycolysis IV |
Glycolysis / Gluconeogenesis | Pentose phosphate pathway | Fructose and mannose metabolism | Carbon fixation |
Intermediary Carbon Metabolism |
|
|
|
2.71 |
4.33 |
At1g22410 |
0.582 |
|
Similar to 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase from Nicotiana tabacum |
-1 |
1.5 |
1.1 |
-0.1 |
-0.7 |
-1 |
-0.8 |
-0.8 |
-0.4 |
-0.5 |
-1 |
2 |
1.9 |
1.7 |
1.1 |
0.7 |
-0.2 |
-0.7 |
-0.9 |
0.9 |
1.1 |
-1.8 |
1.4 |
0.3 |
-0.5 |
0.3 |
-0.9 |
-0.7 |
-0.3 |
-0.8 |
-0.3 |
0 |
0.7 |
-0.1 |
0.4 |
0.2 |
0.3 |
0.3 |
0 |
0.2 |
0.3 |
0.4 |
0.3 |
0.1 |
0 |
0.2 |
0.3 |
0.3 |
0.4 |
-0.4 |
-0.2 |
0 |
0.5 |
-0.1 |
-0.5 |
-1.3 |
1.5 |
1.1 |
0.2 |
0 |
1.7 |
1.4 |
1.9 |
1.1 |
0 |
-0.2 |
0.2 |
0.2 |
-0.2 |
-0.5 |
-0.4 |
0 |
0 |
-0.2 |
-0.5 |
0 |
0.1 |
0 |
0.1 |
-0.1 |
-0.3 |
-0.2 |
-0.1 |
0 |
-0.1 |
-0.2 |
0.1 |
-0.4 |
0.1 |
-0.8 |
-1.2 |
1 |
-0.4 |
-1.1 |
1.1 |
1.3 |
0.3 |
1.8 |
-1 |
-0.5 |
1.5 |
1.4 |
1.7 |
1 |
1.8 |
2.3 |
0 |
1 |
0.8 |
0 |
0 |
0 |
-0.3 |
-0.2 |
-0.2 |
-0.1 |
0 |
0 |
-0.3 |
-0.1 |
0 |
0 |
0.1 |
0.9 |
0 |
0.6 |
0.2 |
-0.3 |
-0.4 |
0 |
0 |
0 |
-0.4 |
0.4 |
0.9 |
1.7 |
0.5 |
2 |
-0.2 |
0 |
-0.2 |
0.2 |
0.3 |
-1.3 |
-1.6 |
-3.7 |
1.1 |
-0.5 |
0.1 |
0.8 |
0.4 |
0 |
0.1 |
0 |
0 |
-0.2 |
-1.4 |
-1.2 |
-1.4 |
-2 |
-1.3 |
-1.8 |
-1.5 |
-1.5 |
-3.3 |
-3.6 |
-1.6 |
At1g22410 |
261933_at |
|
Similar to 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase from Nicotiana tabacum |
6 |
aromatic amino acid family biosynthesis, shikimate pathway |
|
homocysteine and cysteine interconversion |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
3.28 |
6.08 |
At4g01850 |
0.581 |
SAM2 |
S-adenosylmethionine synthetase 2 |
1.1 |
1 |
1.1 |
1.1 |
1.5 |
1.1 |
1.3 |
1.1 |
1.3 |
1.3 |
1.2 |
1.3 |
1.5 |
1.5 |
1.3 |
1.2 |
1.3 |
1.1 |
1.2 |
0.9 |
1 |
0 |
0 |
0 |
0.1 |
0.5 |
0.6 |
0.8 |
0.5 |
0.7 |
0.5 |
0.3 |
0 |
0.3 |
0 |
0.3 |
-0.1 |
0 |
0 |
0 |
0 |
-0.1 |
0.1 |
0 |
0 |
-0.1 |
-0.4 |
-0.3 |
0 |
0.2 |
-0.1 |
-0.2 |
0.1 |
0.6 |
-0.4 |
-0.5 |
-0.1 |
0 |
0 |
-0.3 |
-0.6 |
-0.2 |
-0.5 |
0.3 |
-0.9 |
-0.8 |
-0.7 |
-0.3 |
-0.4 |
-0.3 |
-0.3 |
-0.5 |
-0.4 |
-0.8 |
-1.1 |
0.2 |
-0.2 |
-0.3 |
-0.4 |
-0.2 |
-0.1 |
0.2 |
0.1 |
0 |
-0.5 |
-0.4 |
0.4 |
-1.6 |
-1.5 |
-0.9 |
-0.4 |
0.9 |
0.1 |
-0.6 |
0.4 |
0.6 |
-0.2 |
0.9 |
-0.5 |
-0.2 |
0.8 |
0.7 |
0.8 |
1.1 |
1.7 |
1 |
-0.2 |
1 |
0.3 |
0.5 |
0.2 |
0 |
-0.3 |
0 |
-0.1 |
-0.2 |
-0.6 |
-0.4 |
-0.5 |
-0.4 |
-0.1 |
-0.1 |
0.2 |
-0.1 |
-0.2 |
0 |
0.2 |
-0.7 |
-0.5 |
-0.1 |
-0.2 |
0.4 |
-0.2 |
-0.5 |
1.1 |
0.2 |
0.7 |
0.1 |
-0.1 |
0.1 |
0.5 |
-0.6 |
-0.8 |
-1.4 |
-2 |
-2.1 |
0.4 |
-0.1 |
0.6 |
0.3 |
0.1 |
-0.4 |
-0.4 |
-0.3 |
-0.8 |
-1 |
-2.4 |
-2.2 |
-1.2 |
-0.7 |
-2.3 |
-1.8 |
0 |
0 |
-1.3 |
-1.1 |
-0.4 |
At4g01850 |
255552_at |
SAM2 |
S-adenosylmethionine synthetase 2 |
10 |
|
amino acid metabolism |
methionine and S-adenosylmethionine synthesis | methionine degradation I |
Methionine metabolism | Selenoamino acid metabolism |
Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate |
|
|
|
2.71 |
4.19 |
At1g11580 |
0.575 |
|
similar to pectin methylesterase (Lycopersicon esculentum) |
1.3 |
0.3 |
0.7 |
0.5 |
0.7 |
0.7 |
0.8 |
0.6 |
0.5 |
0.7 |
2.9 |
1.7 |
0.4 |
1.1 |
0.7 |
0.9 |
1.1 |
0.4 |
2.4 |
0 |
1.3 |
-1.9 |
0.6 |
1 |
0.2 |
3.6 |
3.8 |
3.7 |
3.7 |
3.4 |
3.7 |
0.8 |
2.5 |
0.8 |
1.1 |
2.4 |
0.6 |
0.7 |
0.5 |
0.2 |
0.3 |
0.6 |
0.9 |
0.2 |
0.2 |
0.7 |
0.4 |
0.5 |
0.3 |
0.5 |
-0.8 |
0 |
2.5 |
-1 |
-0.2 |
-1.3 |
-0.7 |
-1.1 |
-0.1 |
-0.6 |
-1.7 |
-1 |
1 |
4.2 |
-1.2 |
-1.4 |
-0.6 |
-0.4 |
-0.6 |
-0.6 |
-0.3 |
-0.3 |
-0.2 |
-1.3 |
-1.3 |
1.7 |
0.8 |
0.1 |
0.4 |
0.7 |
0.4 |
0 |
-0.1 |
1.6 |
0 |
-0.1 |
0.9 |
-1.7 |
-1.1 |
-1.7 |
-0.4 |
3.4 |
-0.6 |
-0.5 |
3.9 |
2.9 |
2.5 |
3.2 |
-2.5 |
-2.6 |
2.5 |
2.6 |
3.3 |
-0.3 |
0 |
0.4 |
-0.7 |
1.4 |
-0.1 |
0 |
0.1 |
-1.1 |
-0.5 |
-0.3 |
-0.3 |
-1.1 |
0.2 |
0.2 |
-0.5 |
-0.8 |
-2 |
-1.8 |
-0.8 |
-1.4 |
-1 |
-1.8 |
-1.5 |
-1.8 |
-0.9 |
-1.6 |
-0.7 |
-1.4 |
-2.6 |
-1.9 |
-1.8 |
-1.1 |
-1 |
-1.4 |
-0.7 |
-0.8 |
-1.3 |
-2.6 |
-2.6 |
-2.6 |
-2.6 |
-2.6 |
-0.8 |
-0.2 |
-0.2 |
-0.4 |
-1.2 |
-1.9 |
-2.6 |
-2.2 |
-2.3 |
-2.4 |
-3.3 |
-3.2 |
0.1 |
2.1 |
-2.6 |
-2.6 |
0.6 |
0.6 |
0.2 |
-0.1 |
2.9 |
At1g11580 |
261826_at |
|
similar to pectin methylesterase (Lycopersicon esculentum) |
4 |
|
|
|
|
Cell Wall Carbohydrate Metabolism | pectin metabolism |
|
|
|
6.13 |
7.63 |
At1g48850 |
0.575 |
|
Similar to chorismate synthase from Lycopersicon esculentum |
0.4 |
1.9 |
1.7 |
1 |
0.5 |
0.5 |
0.4 |
0.4 |
0.5 |
0.4 |
0.4 |
2.4 |
2.3 |
2 |
1.7 |
1.2 |
0.6 |
0.3 |
0.2 |
0.2 |
0.6 |
-0.2 |
2.4 |
0.8 |
0 |
0.5 |
-0.3 |
-0.1 |
0 |
-0.2 |
0 |
0.2 |
-0.3 |
0.3 |
-0.5 |
0 |
0.2 |
-0.3 |
-0.4 |
0 |
0.1 |
0.2 |
0 |
-0.3 |
-0.1 |
-0.1 |
0.1 |
0 |
0.1 |
-0.3 |
-0.5 |
-0.3 |
0.4 |
-0.6 |
-0.8 |
-0.9 |
1.3 |
1.2 |
-0.2 |
-0.7 |
1.1 |
1 |
0.9 |
0.6 |
-0.3 |
-0.3 |
-0.3 |
0 |
-0.1 |
-0.7 |
-0.5 |
-0.3 |
-0.4 |
-0.7 |
-0.6 |
-0.1 |
0 |
-0.2 |
-0.1 |
0 |
0 |
-0.4 |
-0.5 |
-0.3 |
-0.5 |
-0.6 |
-1 |
-1 |
-0.7 |
-0.8 |
-0.7 |
0.5 |
-0.9 |
-1.1 |
-0.2 |
0.8 |
-0.7 |
1.4 |
-1.5 |
-1.5 |
1.2 |
1.1 |
1.3 |
0 |
1 |
0.3 |
-0.5 |
0.7 |
-1.2 |
0.1 |
0.1 |
0 |
-0.1 |
0 |
0.1 |
0 |
-0.1 |
-0.1 |
-0.1 |
-0.1 |
0.3 |
0.3 |
0.5 |
0 |
-0.2 |
-0.1 |
-0.2 |
-0.8 |
-0.6 |
-0.3 |
0.1 |
-0.6 |
0 |
0.2 |
0.9 |
-0.6 |
0.4 |
-0.1 |
0 |
-0.2 |
-0.2 |
-0.8 |
-0.8 |
-0.1 |
0 |
0 |
0.2 |
-0.4 |
-0.1 |
0 |
-0.3 |
-0.7 |
-0.5 |
-1 |
-1.1 |
-1.2 |
-0.2 |
-0.2 |
-0.6 |
-0.2 |
-0.4 |
-0.1 |
-0.8 |
-0.8 |
-0.7 |
-0.8 |
0 |
At1g48850 |
245832_at |
|
Similar to chorismate synthase from Lycopersicon esculentum |
6 |
aromatic amino acid family biosynthesis, shikimate pathway |
|
chorismate biosynthesis |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
2.38 |
4.03 |
At4g13660 |
0.572 |
|
similar to pinoresinol-lariciresinol reductase TH1 (Tsuga heterophylla) |
2.3 |
1.5 |
2.3 |
2.7 |
2.6 |
2.2 |
1.9 |
1.5 |
1.4 |
1.1 |
4.2 |
3.5 |
3.4 |
3.4 |
3.1 |
2.8 |
2.8 |
1.5 |
1.7 |
2.7 |
2.5 |
3.2 |
2 |
1.5 |
0.7 |
2.3 |
2.2 |
2.2 |
2.3 |
2.2 |
2.2 |
1.7 |
2.6 |
1.7 |
1.9 |
2.8 |
2.8 |
2.6 |
2.4 |
2.5 |
2.3 |
2.2 |
2.2 |
2.1 |
2.2 |
2.1 |
2.1 |
2.2 |
1.9 |
2.3 |
3.1 |
-1.6 |
1.6 |
-0.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
0.9 |
2.1 |
3.4 |
3 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
1.9 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
3.3 |
-1.6 |
-1.6 |
4.3 |
3.8 |
2.9 |
4.6 |
-1.6 |
-1.6 |
3.7 |
3.4 |
4.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
-1.6 |
0.5 |
0.5 |
-1.6 |
-1.6 |
1.7 |
At4g13660 |
254726_at |
|
similar to pinoresinol-lariciresinol reductase TH1 (Tsuga heterophylla) |
4 |
|
|
|
Propanoate metabolism | Fatty acid biosynthesis (path 2) | Tryptophan metabolism | 1,1,1-Trichloro-2,2-bis(4-chlorophenyl)ethane (DDT) degradatio |
|
|
|
|
5.15 |
6.34 |
At4g39980 |
0.572 |
DHS1 |
2-dehydro-3-deoxyphosphoheptonate aldolase 1 / 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase 1 / DAHP synthetase 1 (DHS1) |
-0.5 |
1.6 |
0.6 |
0.1 |
0.3 |
0.1 |
0.3 |
0.4 |
0.6 |
0.5 |
0.1 |
2.6 |
2.1 |
2 |
1.5 |
1.3 |
0.7 |
0.7 |
0.6 |
-0.1 |
0.1 |
-0.2 |
2 |
-0.2 |
-0.9 |
0.4 |
0.4 |
0.1 |
0.2 |
0.2 |
0.2 |
-0.7 |
-0.4 |
-0.8 |
-0.2 |
0 |
-1.1 |
-0.6 |
-0.4 |
-0.3 |
-0.6 |
-0.7 |
-0.9 |
-0.6 |
-0.3 |
-0.3 |
-0.4 |
-0.8 |
-0.9 |
-0.2 |
-1.1 |
0 |
0.5 |
-0.6 |
-0.5 |
0.3 |
2.2 |
1.9 |
2 |
0.8 |
1.4 |
1 |
0.7 |
0.9 |
0.3 |
-0.1 |
0.1 |
-0.3 |
-1 |
-1.7 |
-1.3 |
0 |
0.2 |
0.8 |
0.1 |
-0.1 |
0.3 |
0.8 |
0.9 |
0 |
-0.5 |
-0.1 |
0 |
0.4 |
0.1 |
0 |
0.6 |
-0.3 |
-0.3 |
-0.8 |
-1.2 |
0.8 |
1.3 |
0.5 |
0.8 |
0.1 |
-0.1 |
0.8 |
-0.6 |
-0.1 |
0.6 |
0.9 |
0.8 |
0.6 |
0.1 |
0.4 |
-0.3 |
0.2 |
0.3 |
0.5 |
0.6 |
0.4 |
0.4 |
0.1 |
0 |
-0.2 |
0.6 |
0.2 |
0 |
0 |
-0.1 |
0 |
0.1 |
-0.7 |
-0.4 |
-0.7 |
0 |
-0.6 |
-0.5 |
0.1 |
0.2 |
0.3 |
-0.4 |
-0.8 |
0.7 |
-2.6 |
-0.4 |
-2.7 |
0 |
0.1 |
-0.4 |
-0.2 |
-0.2 |
-1.4 |
-1.6 |
-3.1 |
0 |
-1.2 |
-0.2 |
0.5 |
0.5 |
0.8 |
1.1 |
0 |
0 |
-0.3 |
-1.6 |
-1.3 |
-0.7 |
0.2 |
-1.4 |
-1.2 |
-1.3 |
-1.3 |
-0.3 |
-0.7 |
0 |
At4g39980 |
252831_at |
DHS1 |
2-dehydro-3-deoxyphosphoheptonate aldolase 1 / 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase 1 / DAHP synthetase 1 (DHS1) |
10 |
response to pathogenic bacteria | response to wounding | 3-deoxy-7-phosphoheptulonate synthase activity | chloroplast | aromatic amino acid family biosynthesis, shikimate pathway |
|
|
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
2.88 |
5.72 |
At4g08770 |
0.567 |
|
peroxidase, putative, identical to class III peroxidase ATP38 (Arabidopsis thaliana) |
2.7 |
4.5 |
3.7 |
4 |
3.7 |
3.4 |
3.2 |
3.3 |
3.3 |
3.1 |
0.1 |
2.9 |
3.8 |
4.4 |
4.1 |
3.9 |
3.6 |
2.6 |
4.1 |
3.1 |
4.3 |
-1.7 |
3.3 |
1.5 |
-0.2 |
4.5 |
3.7 |
3.5 |
4.3 |
3.6 |
4.2 |
1.2 |
2.5 |
0 |
1.8 |
2.8 |
0 |
0 |
0.1 |
0 |
0 |
-0.3 |
0 |
-0.2 |
0 |
0.6 |
-1.7 |
-0.8 |
0.8 |
0.3 |
-0.4 |
-1.7 |
1.4 |
2.1 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
1.9 |
3 |
3.8 |
4.7 |
-0.6 |
-1.7 |
-0.6 |
0 |
-1.7 |
-1.7 |
-1.7 |
-0.5 |
-1.7 |
-1.7 |
-1.7 |
1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
0.1 |
-1.2 |
-1.7 |
-1.7 |
2.5 |
2.5 |
3.3 |
5.4 |
3.9 |
1.4 |
4.9 |
-1.7 |
-1.7 |
3.4 |
3.2 |
5 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.5 |
-1.4 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-0.9 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-1.7 |
-0.9 |
-0.9 |
-1.7 |
-1.7 |
-0.9 |
At4g08770 |
255110_at |
|
peroxidase, putative, identical to class III peroxidase ATP38 (Arabidopsis thaliana) |
2 |
|
disease, virulence and defense | detoxification |
|
Methane metabolism | Prostaglandin and leukotriene metabolism | Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis |
|
|
|
|
6.03 |
7.17 |
At5g22630 |
0.561 |
|
prephenate dehydratase family protein |
0 |
1.3 |
-1.8 |
-2.8 |
-1.9 |
-2.4 |
-1.9 |
-1.9 |
-1.7 |
-2.4 |
-1.5 |
2.4 |
0.7 |
0.7 |
-0.6 |
-1.5 |
-2.8 |
-2.8 |
-2.8 |
-1.5 |
0 |
-1.6 |
0.6 |
-0.1 |
-1.6 |
1.4 |
0.4 |
0.9 |
1.4 |
0.7 |
1.3 |
0.7 |
1.6 |
0.5 |
-0.1 |
0.8 |
1.1 |
0.4 |
0.4 |
0.9 |
0.8 |
0.7 |
0.7 |
1 |
0.8 |
0.7 |
0.7 |
0.7 |
0.7 |
-0.4 |
0.1 |
0.3 |
0.8 |
-0.6 |
-0.3 |
0.3 |
-0.2 |
-0.2 |
2.9 |
2.4 |
1.1 |
0.1 |
1.8 |
1.4 |
-0.7 |
-0.5 |
0.2 |
-0.4 |
-1 |
-0.5 |
0.3 |
0 |
-0.4 |
-0.4 |
-0.8 |
0.3 |
-0.5 |
-0.8 |
-0.6 |
-1.3 |
-0.7 |
-2.1 |
-1.7 |
0.7 |
0 |
0.1 |
1.7 |
-0.1 |
0.2 |
0.1 |
0 |
2 |
0.5 |
0.6 |
2.1 |
2.7 |
3.3 |
2.8 |
-0.1 |
-0.1 |
2.6 |
2.9 |
2.7 |
1.9 |
3.3 |
3 |
-0.5 |
1.8 |
2.6 |
0.8 |
0.5 |
-0.3 |
-0.9 |
-0.9 |
-0.7 |
-0.4 |
-1.8 |
-1.2 |
-1.2 |
-0.7 |
0.2 |
0.6 |
0.6 |
1 |
0.4 |
2.1 |
-0.5 |
-0.4 |
-0.7 |
0 |
0.1 |
-0.7 |
0.8 |
0.9 |
1.5 |
2.1 |
1.3 |
1.9 |
0.5 |
0.4 |
-0.2 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
1.9 |
-0.4 |
0.2 |
2.1 |
1.6 |
0.8 |
1.2 |
1.2 |
0.8 |
0.7 |
-2.7 |
-2.5 |
-2.8 |
-2.8 |
-2.7 |
-2.8 |
-1.7 |
-1.7 |
-2.8 |
-2.8 |
-2.8 |
At5g22630 |
249910_at |
|
prephenate dehydratase family protein |
4 |
|
|
phenylalanine biosynthesis II | tyrosine biosynthesis I |
|
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | Phe biosynthesis |
|
5.47 |
6.21 |
At1g28680 |
0.558 |
|
transferase family protein, similar to elicitor inducible gene product EIG-I24 (Nicotiana tabacum) |
-1 |
0.2 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
0.9 |
0 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
-1 |
0 |
0.8 |
-0.3 |
0.8 |
-0.4 |
-0.1 |
0 |
0 |
0 |
0.8 |
0.7 |
0.4 |
0.6 |
0.6 |
0.7 |
0.6 |
0.3 |
0.6 |
1 |
1 |
0.6 |
0.5 |
0.2 |
0.7 |
0.7 |
0.4 |
0.8 |
0 |
0 |
-0.5 |
0.8 |
-0.1 |
-0.1 |
-0.3 |
0.6 |
0.8 |
0.1 |
-0.3 |
1 |
0.9 |
1.3 |
1 |
0.1 |
0 |
-0.2 |
-0.1 |
-0.2 |
-0.2 |
0 |
0.3 |
0.1 |
0.1 |
0.3 |
0.3 |
0 |
-0.3 |
0.2 |
-0.1 |
-0.3 |
0.6 |
0.5 |
-0.7 |
-0.7 |
-0.7 |
-0.1 |
-0.2 |
-0.1 |
0.3 |
-0.5 |
1.1 |
1.7 |
1.4 |
1.3 |
2.1 |
0.7 |
3.1 |
-0.7 |
-0.2 |
2.4 |
2.2 |
3.1 |
-0.3 |
0.7 |
0.7 |
-0.2 |
1.2 |
0.5 |
-0.1 |
-0.3 |
-0.4 |
-0.2 |
0.1 |
-0.2 |
-0.2 |
0.6 |
0.1 |
-0.1 |
-0.2 |
0 |
-0.4 |
-0.2 |
-0.2 |
-0.1 |
0 |
0.4 |
-0.1 |
0 |
-0.7 |
-0.2 |
-0.8 |
-0.9 |
-0.1 |
0.4 |
-0.5 |
-0.7 |
0 |
-0.3 |
-0.4 |
-0.5 |
-1 |
-1 |
-1 |
-1 |
-1 |
0.7 |
0.1 |
0.5 |
0.4 |
-0.1 |
0 |
-0.1 |
-0.8 |
-0.8 |
-0.7 |
-1 |
-1 |
-1 |
0.5 |
-1 |
-1 |
-0.1 |
-0.1 |
-0.6 |
-1 |
0.4 |
At1g28680 |
262744_at |
|
transferase family protein, similar to elicitor inducible gene product EIG-I24 (Nicotiana tabacum) |
1 |
|
|
|
|
|
|
|
acyltransferase, BAHD family, group A, taxol-like |
2.37 |
4.22 |
At4g23650 |
0.556 |
CDPK6 |
member of Calcium Dependent Protein Kinase |
0.9 |
1.1 |
1.2 |
1 |
0.9 |
0.8 |
1 |
0.9 |
1.1 |
1.3 |
0.4 |
0.8 |
1.2 |
1.2 |
1.1 |
0.9 |
0.7 |
0.8 |
0.8 |
0.3 |
0.6 |
0.3 |
0.9 |
0.1 |
0 |
0.7 |
0.6 |
0.6 |
0.5 |
0.5 |
0.6 |
0.3 |
0 |
0 |
0.1 |
0.3 |
0 |
-0.2 |
-0.3 |
-0.4 |
-0.2 |
-0.1 |
-0.2 |
-0.3 |
-0.4 |
-0.3 |
-0.4 |
-0.2 |
-0.4 |
0 |
-0.1 |
0 |
0.5 |
0.5 |
-0.4 |
-0.1 |
-0.1 |
-0.3 |
0.3 |
0.3 |
0.1 |
0.3 |
0.1 |
0.5 |
0.5 |
0.3 |
0.4 |
0.2 |
0.3 |
0.6 |
0.6 |
0.4 |
0.3 |
0 |
0.3 |
0.7 |
0.5 |
0.6 |
0.8 |
0.8 |
0.7 |
0.1 |
0.2 |
0.3 |
0.4 |
0.4 |
0.4 |
0.2 |
0.2 |
0 |
0.1 |
1 |
1 |
0.6 |
0.4 |
0.8 |
0.8 |
1.2 |
0.5 |
0.2 |
0.8 |
0.8 |
1.2 |
0.9 |
0.4 |
0.3 |
0.1 |
0.6 |
0 |
0.2 |
0.3 |
0.5 |
0.5 |
0.4 |
0.6 |
0.4 |
0.2 |
0.6 |
0.5 |
0.5 |
0.2 |
0.1 |
-0.1 |
-0.1 |
0 |
0.4 |
0.6 |
0 |
0.2 |
0.4 |
-0.1 |
0.9 |
0 |
0 |
-0.1 |
-0.5 |
-1.1 |
-0.4 |
0.1 |
0.1 |
0.3 |
-4.8 |
-3.5 |
-4.8 |
-4.8 |
-4.8 |
0.1 |
1 |
0.5 |
0 |
-0.1 |
-0.4 |
-0.9 |
-2.7 |
-2.6 |
-2.9 |
-4.1 |
-4.2 |
-2.3 |
-0.5 |
-4.1 |
-3.6 |
-0.3 |
-0.3 |
-1.5 |
-1.5 |
-0.3 |
At4g23650 |
254224_at |
CDPK6 |
member of Calcium Dependent Protein Kinase |
9 |
N-terminal protein myristoylation | N-terminal protein myristoylation |
intracellular signalling |
|
Inositol phosphate metabolism | Nicotinate and nicotinamide metabolism | Benzoate degradation via CoA ligation |
|
|
|
|
4.48 |
6.10 |
At5g11670 |
0.554 |
|
malate oxidoreductase, putative, similar to NADP-dependent malic enzyme (Phaseolus vulgaris) |
0.2 |
1.6 |
0.7 |
0.1 |
0.5 |
0.3 |
0.5 |
0.4 |
0.4 |
0.2 |
0.5 |
0.8 |
1 |
1 |
0.6 |
0.2 |
0.6 |
0 |
0.5 |
1.2 |
1.9 |
1.3 |
2.4 |
-0.2 |
0 |
0.1 |
0 |
-0.1 |
0 |
-0.2 |
0 |
0.1 |
1.6 |
-0.7 |
0.6 |
1.6 |
-0.2 |
0.2 |
0.7 |
0.8 |
0.3 |
-0.3 |
-0.1 |
0.1 |
0.6 |
0.7 |
0.3 |
0 |
0.2 |
0.3 |
-0.5 |
0.7 |
1.6 |
1.3 |
-0.4 |
1.4 |
2.1 |
1.5 |
2.1 |
2 |
2.1 |
1.4 |
1.8 |
0 |
1.6 |
1.1 |
1.5 |
1.6 |
0.8 |
0 |
0.1 |
0.3 |
0.6 |
1.5 |
1.6 |
0.2 |
-0.4 |
0.7 |
0.6 |
0.3 |
-0.6 |
-1.5 |
-1.6 |
1.1 |
0.9 |
0.9 |
0.5 |
1.3 |
1.2 |
1.7 |
1.3 |
1.4 |
1.9 |
1.3 |
1.3 |
1.1 |
2.7 |
1.9 |
-0.6 |
-0.6 |
1.6 |
1.4 |
1.8 |
-0.1 |
0.8 |
0.8 |
-0.7 |
0.7 |
1.5 |
-0.1 |
0 |
-0.9 |
-0.6 |
-1.4 |
-1.6 |
-1.5 |
-0.2 |
-1.1 |
-1.2 |
-1.1 |
-0.6 |
-0.6 |
-0.4 |
0.3 |
-0.9 |
-0.1 |
-0.7 |
-0.9 |
-0.5 |
-0.5 |
-0.3 |
-0.9 |
0 |
0.5 |
-0.9 |
1 |
-0.8 |
0.3 |
-0.4 |
-0.2 |
-0.4 |
-4.8 |
-4.8 |
-4.8 |
-4.8 |
-4.8 |
0 |
0.8 |
-0.5 |
0 |
-0.1 |
-1.4 |
-1.2 |
-2.1 |
-1.6 |
-2 |
-3.2 |
-3.7 |
-1.9 |
-2.3 |
-3.7 |
-3.2 |
-0.4 |
-0.4 |
-3.2 |
-3.7 |
-2.1 |
At5g11670 |
250339_at |
|
malate oxidoreductase, putative, similar to NADP-dependent malic enzyme (Phaseolus vulgaris) |
4 |
|
C-compound and carbohydrate metabolism | tricarboxylic-acid pathway (citrate cycle, Krebs cycle, TCA cycle) | photosynthesis |
|
Pyruvate metabolism | Carbon fixation |
Intermediary Carbon Metabolism |
|
|
|
5.17 |
7.58 |
At1g53310 |
0.546 |
ATPPC1 |
strong similarity to Phosphoenolpyruvate carboxylase from Solanum tuberosum |
0 |
-0.1 |
0 |
0.1 |
0.2 |
0.3 |
0.2 |
0.1 |
0.3 |
0.4 |
-0.7 |
0.7 |
0.9 |
0.7 |
0.2 |
0.3 |
-0.1 |
0.1 |
0.6 |
1.1 |
1.5 |
-0.2 |
-0.7 |
0.3 |
-1.4 |
0.6 |
0 |
-0.1 |
-0.1 |
-0.2 |
0 |
-0.2 |
1.4 |
-0.3 |
0 |
0.9 |
0.1 |
0 |
-0.2 |
0 |
0.2 |
0 |
0 |
0 |
0 |
0.1 |
0 |
0 |
0.2 |
-1.2 |
-1.2 |
0 |
0.5 |
-0.5 |
-1.1 |
-1.1 |
1.3 |
1.2 |
-0.7 |
-1.1 |
2.5 |
2.1 |
1.8 |
1.2 |
0.3 |
0 |
-0.1 |
-0.3 |
-0.4 |
-0.9 |
-0.5 |
-0.3 |
-0.1 |
0.3 |
0.3 |
-0.4 |
-0.1 |
0.1 |
0.5 |
-0.4 |
-0.4 |
-0.4 |
-0.5 |
0 |
-0.1 |
-0.3 |
-0.1 |
0.5 |
0.8 |
0.8 |
0 |
0.8 |
0 |
-0.5 |
0.9 |
1 |
0.4 |
1.4 |
-0.3 |
0 |
1.1 |
1 |
1.5 |
0 |
-0.1 |
0.2 |
0.4 |
0.5 |
0.1 |
0 |
0.1 |
0.1 |
0.2 |
0 |
0.1 |
0 |
0.2 |
0.3 |
0.2 |
0.1 |
-0.2 |
-0.1 |
-0.1 |
0.1 |
0 |
0.2 |
0.5 |
-0.2 |
0 |
-0.2 |
-0.2 |
-0.3 |
-0.4 |
0.6 |
0.4 |
0 |
-0.5 |
0 |
0.2 |
0.3 |
0.1 |
-2.1 |
-2.3 |
-2.6 |
-2.6 |
-2.6 |
-0.3 |
0.3 |
-0.4 |
0 |
0 |
-0.1 |
-0.4 |
-1.6 |
-1.3 |
-1.4 |
-0.6 |
-0.4 |
-0.7 |
-0.1 |
-0.6 |
-0.2 |
0 |
0 |
0.1 |
0 |
0 |
At1g53310 |
260590_at |
ATPPC1 |
strong similarity to Phosphoenolpyruvate carboxylase from Solanum tuberosum |
6 |
|
C-compound and carbohydrate metabolism | glycolysis and gluconeogenesis |
gluconeogenesis | asparagine degradation I | aspartate degradation I | phenylalanine degradation I | serine-isocitrate lyase pathway | formaldehyde assimilation I (serine pathway) | mixed acid fermentation | acetyl-CoA assimilation | TCA cycle variation VII | TCA cycle variation VIII | TCA cycle variation II | TCA cycle variation IV |
Pyruvate metabolism | Carbon fixation | Reductive carboxylate cycle (CO2 fixation) |
Intermediary Carbon Metabolism |
|
|
|
2.57 |
5.19 |
At1g80360 |
0.546 |
|
aminotransferase class I and II family protein, low similarity to Aromatic Aminotransferase from Pyrococcus horikoshii |
0.2 |
0.6 |
0.7 |
0.8 |
0.4 |
0.5 |
0.4 |
0.4 |
0.3 |
0 |
1.3 |
1.3 |
1.2 |
0.8 |
0.3 |
0.2 |
0.4 |
0.3 |
0.1 |
-0.2 |
0 |
0.5 |
0.3 |
0.2 |
0 |
0 |
0 |
0 |
0 |
0 |
-0.1 |
0.2 |
0.1 |
0 |
0 |
0 |
-0.3 |
0.1 |
0 |
-0.4 |
0.3 |
0.4 |
0.1 |
0.2 |
0.1 |
-0.2 |
0.3 |
0 |
0.1 |
0.2 |
0.2 |
-0.2 |
0.2 |
0 |
-0.5 |
-0.6 |
0 |
0 |
-0.4 |
-0.7 |
0.8 |
0.9 |
1.7 |
1 |
-0.2 |
-0.4 |
0 |
-0.1 |
-0.3 |
0 |
0 |
0 |
0 |
-0.1 |
-0.3 |
0.1 |
-0.1 |
-0.2 |
-0.2 |
0 |
-0.1 |
0 |
-0.2 |
-0.2 |
-0.3 |
-0.4 |
-0.1 |
-0.4 |
-0.6 |
0 |
0.2 |
0.6 |
0.8 |
0.7 |
0.4 |
0.6 |
-0.2 |
1 |
-0.6 |
-0.2 |
0.7 |
0.7 |
1.2 |
-1.2 |
0 |
0.3 |
0.1 |
0 |
0 |
-0.2 |
-0.1 |
0 |
-0.4 |
-0.2 |
-0.1 |
-0.1 |
-0.2 |
0 |
-0.1 |
0 |
-0.1 |
-0.3 |
-0.1 |
0 |
0 |
0.4 |
0 |
0.2 |
0.2 |
-1.2 |
-0.3 |
0 |
0 |
1 |
-0.3 |
0.9 |
0.2 |
0.2 |
-0.3 |
-0.2 |
-0.6 |
-0.5 |
-0.6 |
-0.3 |
-0.5 |
-0.3 |
0.3 |
0.2 |
-0.3 |
0.1 |
0 |
-0.3 |
-0.2 |
-1 |
-0.8 |
-0.9 |
-1.3 |
-0.9 |
0 |
-0.5 |
-0.8 |
-1 |
-0.4 |
-0.4 |
-1 |
-1 |
-0.7 |
At1g80360 |
260328_at |
|
aminotransferase class I and II family protein, low similarity to Aromatic Aminotransferase from Pyrococcus horikoshii |
2 |
|
|
phenylalanine biosynthesis II |
|
|
|
|
|
1.80 |
3.08 |
At5g05160 |
0.546 |
|
leucine-rich repeat transmembrane protein kinase, putative, |
2 |
0.3 |
1.8 |
2.2 |
2 |
2 |
1.7 |
1.8 |
1.7 |
1.6 |
0.4 |
3 |
3.5 |
3.3 |
3.6 |
4 |
3.6 |
2.7 |
3.3 |
4 |
4.2 |
-2.1 |
1.1 |
0.5 |
-2.1 |
1.1 |
0 |
-1.2 |
-1 |
-2.1 |
-0.9 |
-0.3 |
1.9 |
0.1 |
0.4 |
0.6 |
1.1 |
0.5 |
0.8 |
1 |
1.3 |
1.3 |
1.1 |
0.9 |
0.6 |
1.1 |
1.1 |
1 |
0.7 |
-2.1 |
-0.4 |
-1.2 |
3.1 |
-1 |
0.5 |
0.3 |
0.1 |
0.9 |
0.3 |
0 |
0.4 |
1.6 |
1.3 |
3.5 |
-0.8 |
-0.7 |
-1.5 |
-2.1 |
-2.1 |
-1.3 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
0.6 |
0.1 |
0 |
0.2 |
0 |
0.1 |
-2.1 |
-2.1 |
0.3 |
-0.5 |
-0.2 |
0.1 |
-2.1 |
-2.1 |
-2.1 |
-0.9 |
3.1 |
-2.1 |
-2.1 |
2.1 |
3 |
2.3 |
1.8 |
-2.1 |
-2.1 |
2.6 |
2.7 |
2 |
0.1 |
0.6 |
1.3 |
0.2 |
1.8 |
1.3 |
0.1 |
0.9 |
0 |
1 |
1.1 |
0.6 |
0.6 |
2.1 |
2.1 |
1.9 |
1.6 |
-0.2 |
-0.2 |
-1.1 |
-1.3 |
0.3 |
0.2 |
0.1 |
0.1 |
-0.4 |
-0.2 |
-0.5 |
0.7 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-1 |
-0.2 |
-0.2 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-0.3 |
-2.1 |
-1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
-2.1 |
At5g05160 |
250820_at |
|
leucine-rich repeat transmembrane protein kinase, putative, |
1 |
|
|
|
|
|
|
|
Acyl activating enzymes , CoA ligases, clade IV, 4-coumarate-CoA ligase like |
5.42 |
6.35 |
At3g44720 |
0.544 |
|
prephenate dehydratase family protein |
1.1 |
1.1 |
0 |
0 |
0.2 |
0 |
0 |
0.2 |
0.3 |
0.1 |
0.6 |
2.5 |
1.7 |
1.4 |
0.9 |
0 |
0 |
-1 |
-0.4 |
0.2 |
0.5 |
-0.3 |
1.7 |
-0.1 |
-1.8 |
3.3 |
3.1 |
3.5 |
3.3 |
2.7 |
3 |
0.7 |
0.8 |
0 |
-1.2 |
0 |
-0.1 |
-0.3 |
-0.8 |
-0.4 |
-0.1 |
-0.1 |
-0.2 |
-0.1 |
-0.3 |
-0.4 |
-0.2 |
-0.1 |
0.1 |
0.3 |
-0.2 |
0.3 |
1 |
-0.5 |
0.6 |
0.5 |
1.2 |
0.7 |
2.3 |
2.3 |
2.2 |
1.8 |
2.7 |
2.4 |
-0.3 |
0.6 |
0.9 |
0.5 |
0.6 |
0.9 |
1.3 |
1.1 |
0.1 |
-0.7 |
-0.5 |
0.6 |
-0.8 |
-1.3 |
-1 |
-0.3 |
-0.3 |
-1.4 |
-1.3 |
-0.3 |
0 |
0.2 |
-0.2 |
0.3 |
-0.1 |
0.5 |
0.2 |
0.4 |
0.8 |
-1.4 |
-1.4 |
1.2 |
1.8 |
0.9 |
-0.4 |
-0.9 |
-0.4 |
0.2 |
0.9 |
-0.5 |
1.3 |
0.5 |
-1 |
0.7 |
-1.4 |
0.2 |
0.1 |
-0.2 |
-0.4 |
-0.5 |
-0.5 |
-0.3 |
-2.3 |
-1.8 |
-2 |
-1.6 |
-0.5 |
-0.2 |
0.3 |
-0.6 |
-0.7 |
-1.5 |
-1.6 |
-0.7 |
-1.4 |
-0.7 |
-0.1 |
-1.3 |
-0.6 |
0.3 |
-1.1 |
-1.4 |
1.1 |
-1.4 |
0 |
-0.8 |
-0.7 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
1.1 |
0.2 |
-0.9 |
0.8 |
0.6 |
1.3 |
1.1 |
-0.7 |
-1.3 |
-1.4 |
-1.4 |
-1.4 |
-1.3 |
-1.6 |
-1.4 |
-1.4 |
-0.8 |
-0.8 |
-1.4 |
-1.4 |
-1.4 |
At3g44720 |
252652_at |
|
prephenate dehydratase family protein |
4 |
|
|
phenylalanine biosynthesis II | tyrosine biosynthesis I |
|
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | Phe biosynthesis |
|
3.82 |
5.81 |
At1g20330 |
0.543 |
SMT2 |
S-adenosyl-methionine-sterol-C-methyltransferase. Encodes a sterol-C24-methyltransferases involved in sterol biosynthesis. |
-0.3 |
-1 |
-0.5 |
0.6 |
0.5 |
0.1 |
0 |
0.1 |
0 |
0.2 |
0.6 |
1.4 |
1.6 |
1.6 |
1.5 |
1.5 |
1 |
0.5 |
0.8 |
0.7 |
0.5 |
0 |
0.2 |
0.5 |
1.2 |
0.6 |
0.4 |
0.1 |
0.3 |
0 |
0.4 |
0.8 |
0 |
0.9 |
0.5 |
0 |
0.1 |
0.1 |
0 |
-0.2 |
0 |
0 |
0.4 |
0 |
0 |
0 |
-0.1 |
0.1 |
0.3 |
0.2 |
0.5 |
-0.2 |
-0.2 |
-0.3 |
0.5 |
0.4 |
0.9 |
0.9 |
0.5 |
0.3 |
0.3 |
0.5 |
0.3 |
0.8 |
-0.2 |
0 |
0 |
-0.5 |
-0.4 |
0 |
0.7 |
0.8 |
0.2 |
-0.6 |
-0.8 |
0 |
0 |
-0.3 |
-0.6 |
-1 |
-0.4 |
-0.2 |
0 |
0.3 |
0.3 |
0.5 |
0.1 |
-1.3 |
-1.1 |
-1 |
0 |
0.4 |
-0.6 |
-0.4 |
-1 |
0.3 |
-0.4 |
-0.1 |
-0.2 |
0 |
0 |
0.4 |
-0.1 |
0 |
-0.1 |
-0.6 |
0.6 |
0.5 |
-0.9 |
0.6 |
0.8 |
1.2 |
0.7 |
0.7 |
1 |
0.8 |
0.7 |
0.8 |
0.9 |
0.9 |
0.9 |
0.8 |
0.8 |
0 |
1.1 |
0.7 |
1.5 |
0.3 |
0.6 |
0.2 |
1.2 |
0.1 |
0.6 |
-0.5 |
1.3 |
-0.4 |
-0.7 |
-0.7 |
0.8 |
0.5 |
0.4 |
-4 |
-3.7 |
-4 |
-4 |
-4 |
-0.3 |
-0.7 |
0.7 |
0.4 |
0.6 |
0.6 |
0.3 |
-1.1 |
-1.4 |
-1.6 |
-1.7 |
-1.8 |
-1.4 |
-1.7 |
-2.1 |
-1 |
-0.5 |
-0.5 |
-0.7 |
-1.1 |
-0.7 |
At1g20330 |
255885_at |
SMT2 |
S-adenosyl-methionine-sterol-C-methyltransferase. Encodes a sterol-C24-methyltransferases involved in sterol biosynthesis. |
10 |
S-adenosylmethionine-dependent methyltransferase activity | pattern specification | sterol biosynthesis |
|
sterol biosynthesis |
|
Isoprenoid Biosynthesis in the Cytosol and in Mitochondria | sterol biosynthesis |
|
triterpene, sterol, and brassinosteroid metabolism | sterol biosynthesis |
|
2.89 |
5.72 |
At5g17330 |
0.542 |
GAD |
Encodes one of two isoforms of glutamate decarboxylase. |
3.7 |
4 |
3.4 |
2.9 |
3.6 |
3.9 |
3.7 |
3.5 |
3.7 |
3.9 |
0.9 |
1.6 |
1.7 |
2.1 |
1.7 |
1.9 |
3.1 |
3.9 |
3.9 |
3.6 |
3.8 |
2.6 |
3.8 |
2 |
1.4 |
4 |
3.7 |
4.2 |
4.2 |
3.9 |
3.8 |
2.7 |
3.5 |
2.3 |
3 |
3.2 |
2.8 |
2.5 |
2.3 |
2.2 |
2.1 |
2 |
2.2 |
2 |
1.9 |
2.3 |
2.2 |
2.2 |
2.4 |
2.5 |
2.2 |
-0.8 |
2.7 |
0.9 |
-2.8 |
-2.8 |
0 |
-0.1 |
-2.8 |
-1.3 |
2.8 |
3.2 |
4.2 |
3 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
1.6 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-1.1 |
-2.8 |
-0.9 |
0.1 |
-0.2 |
-1.9 |
4.2 |
4.9 |
4.3 |
4.5 |
4.4 |
4.6 |
5.1 |
-2.8 |
-2.8 |
4.9 |
4.8 |
5 |
-2.1 |
-0.4 |
-2.8 |
-2.8 |
0 |
-1.7 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-1.7 |
-0.1 |
-2.8 |
-1.8 |
0.4 |
-2.8 |
-1.6 |
-2.8 |
-2.8 |
-2.8 |
0.9 |
1.8 |
-2.8 |
-2.4 |
-2.8 |
-1.3 |
-2 |
-0.8 |
-2.5 |
1.2 |
0.9 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-0.9 |
-1.9 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
-2.8 |
2.3 |
2.3 |
-2.8 |
-2.8 |
-2.8 |
At5g17330 |
250090_at |
GAD |
Encodes one of two isoforms of glutamate decarboxylase. |
9 |
calmodulin binding | glutamate decarboxylase activity |
|
glutamate degradation I |
Butanoate metabolism | Glutamate metabolism | Alanine and aspartate metabolism | beta-Alanine metabolism | Taurine and hypotaurine metabolism |
|
|
|
|
7.24 |
8.03 |
At1g06620 |
0.534 |
|
2-oxoglutarate-dependent dioxygenase, putative, similar to tomato ethylene synthesis regulatory protein E8 |
0.5 |
0.8 |
0.9 |
0.4 |
0.2 |
0.5 |
0 |
0.2 |
0.4 |
0.2 |
0.2 |
1.3 |
0.6 |
0.4 |
0 |
-0.3 |
-0.9 |
-1.3 |
-0.9 |
-0.3 |
-0.9 |
-0.9 |
-0.9 |
-0.4 |
-0.9 |
1.9 |
2.2 |
1.5 |
2 |
1.7 |
1.7 |
-0.2 |
0.9 |
-0.7 |
0.5 |
0.9 |
0.3 |
0.4 |
-0.2 |
0.1 |
-0.1 |
0 |
0.5 |
0.3 |
0 |
0.2 |
-0.1 |
0 |
0.5 |
0.4 |
-0.4 |
-0.2 |
0.6 |
1 |
-0.9 |
-0.3 |
0.9 |
1.6 |
2.1 |
1.5 |
0.9 |
1.7 |
2.3 |
1.4 |
-0.9 |
-0.5 |
0.3 |
0.1 |
-0.7 |
-0.9 |
-0.6 |
-0.2 |
-0.9 |
-0.2 |
-0.3 |
1 |
-0.9 |
-0.7 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.1 |
-0.8 |
-0.5 |
1.8 |
-0.1 |
-0.1 |
0.4 |
-0.7 |
1.9 |
-0.1 |
-0.4 |
2 |
1.7 |
1.4 |
0.9 |
-0.9 |
-0.9 |
2.7 |
2.8 |
1.9 |
-0.9 |
-0.9 |
-0.3 |
-0.3 |
0.4 |
0.8 |
0 |
-0.2 |
-1.1 |
0.1 |
-0.2 |
0 |
-0.1 |
0.1 |
0.6 |
0 |
0 |
-0.9 |
-0.7 |
0.2 |
0.9 |
-0.7 |
-0.9 |
-0.9 |
-0.4 |
0.1 |
-0.4 |
-0.1 |
-0.9 |
0 |
1.2 |
-0.9 |
-0.9 |
0.4 |
-0.2 |
0.9 |
0.1 |
-0.3 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.6 |
-0.6 |
-0.9 |
-0.9 |
-1 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.1 |
-0.1 |
-0.9 |
-0.9 |
-1 |
At1g06620 |
262616_at |
|
2-oxoglutarate-dependent dioxygenase, putative, similar to tomato ethylene synthesis regulatory protein E8 |
4 |
response to ethylene stimulus |
|
|
|
|
|
|
|
2.88 |
4.18 |
At1g72700 |
0.531 |
|
haloacid dehalogenase-like hydrolase family protein, similar to Potential phospholipid-transporting ATPase (Homo sapiens) |
-0.3 |
-0.2 |
-0.9 |
-2.3 |
-0.4 |
-0.8 |
-0.8 |
-0.5 |
-0.5 |
-0.8 |
0.5 |
-0.1 |
-0.3 |
-0.6 |
-1.1 |
-0.2 |
-0.9 |
-1 |
-1 |
0 |
-0.6 |
2.6 |
-0.6 |
0 |
-0.5 |
0.9 |
0.3 |
0.7 |
0.8 |
0.5 |
0.7 |
-0.1 |
1.2 |
-0.1 |
0.2 |
0 |
0.8 |
0.8 |
0.6 |
0.9 |
0.7 |
0.7 |
0.5 |
0.6 |
0.5 |
0.8 |
0.8 |
0.2 |
0.3 |
0.2 |
0.1 |
-1.2 |
0.8 |
-1 |
-0.5 |
-0.3 |
0.1 |
-0.1 |
0.2 |
0.2 |
2.2 |
1.1 |
1.5 |
0.8 |
0.5 |
0.1 |
0.1 |
0.1 |
0.2 |
-0.5 |
-0.3 |
-0.1 |
0 |
0.1 |
0.4 |
-0.7 |
-0.6 |
-0.2 |
-0.1 |
-0.6 |
-0.7 |
-1 |
-0.2 |
-0.6 |
-0.7 |
-0.2 |
0.4 |
1.1 |
1.1 |
1.5 |
0 |
1.1 |
0.7 |
0.1 |
1.3 |
2 |
2.2 |
1.6 |
0 |
0.1 |
2 |
2 |
1.4 |
0.7 |
1.1 |
1.9 |
0 |
0.6 |
0.1 |
-0.5 |
-0.3 |
-0.6 |
0.6 |
0.3 |
0 |
0.2 |
0.6 |
0.2 |
0.1 |
0.1 |
-0.4 |
-0.1 |
-0.2 |
0 |
0 |
-0.2 |
0.5 |
0 |
-0.1 |
0 |
-0.2 |
0 |
-0.8 |
0.5 |
0.4 |
0.3 |
0.2 |
-0.2 |
0.2 |
0.2 |
-0.2 |
-2.3 |
-2.3 |
-2.3 |
-2.3 |
-2.3 |
0.1 |
1.5 |
-0.1 |
0 |
0.2 |
0.7 |
1.6 |
0.8 |
1.1 |
0.7 |
-2.3 |
-2.5 |
-1.8 |
-1.9 |
-2.3 |
-2.3 |
-0.3 |
-0.3 |
-2.3 |
-2.3 |
-2 |
At1g72700 |
259910_at |
|
haloacid dehalogenase-like hydrolase family protein, similar to Potential phospholipid-transporting ATPase (Homo sapiens) |
2 |
|
|
|
|
|
Miscellaneous acyl lipid metabolism |
|
|
3.89 |
5.15 |
At4g13940 |
0.531 |
HOG1 |
Encodes a S-adenosyl-L-homocysteine hydrolase required for DNA methylation-dependent gene silencing. |
-0.2 |
0.1 |
0.3 |
0.1 |
0.2 |
0 |
0.2 |
0 |
0.1 |
0.2 |
-0.5 |
0.5 |
0.6 |
0.6 |
0.3 |
0.2 |
0.3 |
0.1 |
0 |
0.1 |
-0.3 |
-0.7 |
0.4 |
0 |
-0.6 |
0.2 |
0.3 |
0.6 |
0.3 |
0.4 |
0.2 |
0 |
0.3 |
0 |
0.4 |
0.3 |
0 |
0.2 |
0.1 |
0.2 |
0.2 |
0 |
0.2 |
0.1 |
0.1 |
0.2 |
0.3 |
0.2 |
0 |
0 |
0 |
-0.4 |
0.3 |
0.4 |
-0.3 |
-0.2 |
0.6 |
0.6 |
0.1 |
0 |
0.3 |
0.6 |
0.1 |
0.9 |
0 |
-0.3 |
-0.3 |
0 |
0 |
0 |
0.2 |
0.1 |
-0.1 |
-0.4 |
-0.2 |
0.3 |
0.1 |
-0.1 |
0 |
0.2 |
0.1 |
0.2 |
0.2 |
0.1 |
-0.2 |
-0.4 |
0.2 |
-0.3 |
-0.3 |
-0.4 |
-0.6 |
0.5 |
0.4 |
-0.2 |
0.5 |
0.1 |
0.4 |
0.4 |
0 |
0.1 |
0 |
0 |
0.3 |
0.5 |
0.6 |
0.5 |
0.1 |
0.2 |
0 |
0.3 |
0.3 |
0.2 |
0 |
0 |
-0.1 |
0 |
0 |
0.1 |
0 |
0 |
0 |
0 |
0 |
-0.3 |
0 |
0.1 |
0.5 |
-0.2 |
-0.2 |
0.2 |
0 |
0.7 |
-0.5 |
-0.7 |
0.3 |
-0.6 |
0 |
-0.6 |
0 |
0 |
0.1 |
0.1 |
0 |
-0.7 |
-0.9 |
-2.2 |
0 |
-0.4 |
0 |
0 |
0 |
0 |
-0.1 |
-1.5 |
-1.6 |
-1.8 |
-1.4 |
-1.6 |
0 |
0 |
-1.7 |
-0.9 |
0.2 |
0.2 |
0.7 |
0.4 |
-0.4 |
At4g13940 |
245356_at |
HOG1 |
Encodes a S-adenosyl-L-homocysteine hydrolase required for DNA methylation-dependent gene silencing. |
10 |
adenosylhomocysteinase activity | methylation-dependent chromatin silencing | posttranscriptional gene silencing |
amino acid metabolism |
chlorophyll biosynthesis | biosynthesis of proto- and siroheme | methionine degradation I |
Methionine metabolism | Selenoamino acid metabolism |
Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate |
|
|
|
1.50 |
3.21 |
At3g29200 |
0.530 |
CM1 |
chorismate mutase, chloroplast |
-0.2 |
0.4 |
-0.2 |
0.1 |
-0.1 |
-0.8 |
-0.2 |
0.1 |
-0.5 |
-0.7 |
0.8 |
1.7 |
1.2 |
1.6 |
0.7 |
0.6 |
-0.2 |
-0.5 |
0 |
-0.2 |
0.9 |
1.6 |
2.6 |
0.7 |
0.4 |
0.4 |
0 |
0.2 |
0.1 |
0.3 |
0 |
1.7 |
-0.4 |
1.2 |
-0.4 |
-0.3 |
0.1 |
-0.5 |
-0.5 |
0 |
0.2 |
0.3 |
0 |
-0.9 |
-0.4 |
0.1 |
0 |
0.2 |
-0.6 |
0.9 |
0.9 |
-0.4 |
-0.2 |
-0.6 |
-0.3 |
-1.5 |
0.4 |
0.3 |
-1.5 |
-1.8 |
0 |
-0.2 |
0.8 |
0.2 |
-0.1 |
-0.4 |
-0.6 |
-0.3 |
-0.1 |
-0.3 |
0.3 |
0.5 |
-0.3 |
-1.1 |
-0.4 |
-0.1 |
-0.2 |
-1 |
0 |
-0.2 |
0.1 |
0.5 |
0.3 |
-0.6 |
-0.7 |
-1.1 |
-0.7 |
-0.6 |
-0.8 |
0.4 |
-0.2 |
-0.5 |
1 |
0.5 |
0.2 |
0.2 |
-1.1 |
1.7 |
-0.6 |
-0.4 |
0.5 |
0.2 |
1.5 |
-0.6 |
1.2 |
0.2 |
-0.2 |
0.5 |
-0.3 |
-0.1 |
-0.2 |
0 |
-1 |
-0.5 |
-0.6 |
-0.4 |
-0.4 |
-0.4 |
-0.6 |
-0.5 |
0.6 |
0.8 |
0.8 |
0.1 |
0.3 |
-0.1 |
-0.1 |
0.5 |
0 |
-0.6 |
0.4 |
0 |
0.4 |
0.8 |
0.9 |
0.4 |
0.8 |
0.1 |
0 |
0 |
0 |
-0.1 |
-0.3 |
-0.9 |
-0.9 |
-0.9 |
0.3 |
0 |
-0.6 |
0.6 |
0.4 |
1.3 |
1.7 |
1 |
0.6 |
0.7 |
-1.1 |
-0.7 |
0.3 |
-1 |
-1 |
-0.7 |
-1 |
-1 |
-0.4 |
-0.4 |
-0.4 |
At3g29200 |
257746_at |
CM1 |
chorismate mutase, chloroplast |
10 |
chorismate mutase activity | aromatic amino acid family biosynthesis, shikimate pathway |
|
phenylalanine biosynthesis II | tyrosine biosynthesis I | ascorbate glutathione cycle |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
2.36 |
4.53 |
At1g15950 |
0.528 |
CCR1 |
Cinnamoyl CoA reductase isoform 1 (CCR1). Involved in lignin biosynthesis. |
-1.1 |
-0.3 |
0 |
-0.9 |
-1.1 |
-1 |
-1 |
-1.1 |
-1.1 |
-1.3 |
0.2 |
1.3 |
0.8 |
0.4 |
-0.1 |
-0.2 |
-1.2 |
-2.1 |
-1.3 |
-0.8 |
-0.3 |
1.1 |
0 |
0.7 |
-0.2 |
0.1 |
0.1 |
0.1 |
0.3 |
0 |
0.2 |
0.8 |
0 |
1 |
-0.5 |
0.3 |
0.6 |
0.5 |
-0.2 |
-0.3 |
0.2 |
0.3 |
0.6 |
0.1 |
-0.4 |
-0.2 |
0.1 |
0.4 |
0.5 |
0.5 |
1 |
0 |
0.7 |
-0.1 |
1.1 |
0.3 |
0.9 |
0.7 |
0.7 |
0.5 |
0.9 |
0.8 |
1.1 |
1.3 |
-0.8 |
-1.3 |
-0.8 |
-0.8 |
-0.5 |
0.2 |
0.9 |
1.3 |
0.8 |
-0.1 |
-0.8 |
0.5 |
0.6 |
-0.3 |
-0.4 |
-0.6 |
0 |
1 |
1 |
-0.3 |
-0.6 |
-0.6 |
0.4 |
0.2 |
0.5 |
0.6 |
0.3 |
-0.4 |
0.2 |
-0.5 |
-0.2 |
0.6 |
1.2 |
1 |
-0.5 |
-0.6 |
1 |
1.2 |
0.9 |
0.8 |
1.7 |
1.9 |
-0.2 |
1.3 |
1.3 |
-0.4 |
-0.2 |
-0.6 |
-0.4 |
-0.4 |
-0.4 |
-0.4 |
0.2 |
-0.1 |
-0.4 |
-0.4 |
-1 |
-1.1 |
-0.8 |
-0.2 |
-0.2 |
0.4 |
0.3 |
-1 |
-0.8 |
-0.5 |
-0.8 |
-0.6 |
-0.2 |
1 |
-1.9 |
0.2 |
-1.4 |
0 |
-0.7 |
-0.6 |
-0.2 |
-2.7 |
-2.7 |
-2.7 |
-2.7 |
-2.7 |
0.5 |
0.7 |
-0.2 |
1.1 |
0.7 |
0.7 |
1 |
1.3 |
1.1 |
1.2 |
0.5 |
0.5 |
0.2 |
-0.3 |
0.6 |
0.6 |
0.8 |
0.8 |
-0.5 |
-0.4 |
0.1 |
At1g15950 |
261792_at |
CCR1 |
Cinnamoyl CoA reductase isoform 1 (CCR1). Involved in lignin biosynthesis. |
10 |
cinnamoyl-CoA reductase activity | lignin biosynthesis |
|
lignin biosynthesis |
|
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
|
2.61 |
4.72 |
At1g80820 |
0.523 |
CCR2 |
cinnamoyl CoA reductase isoform 2. Involved in lignin biosynthesis. |
2.4 |
5.3 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
1.3 |
1.7 |
-0.7 |
-0.7 |
4.9 |
3.8 |
4.1 |
3.1 |
1.9 |
-0.7 |
-0.7 |
-0.7 |
2.7 |
2.9 |
-0.7 |
4.4 |
-0.7 |
-0.7 |
1.2 |
1 |
-0.7 |
1.6 |
-0.7 |
1.6 |
-0.7 |
-0.7 |
0.1 |
-0.7 |
-0.7 |
1.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
2.1 |
-0.7 |
-0.7 |
-0.7 |
1.5 |
0.7 |
3.8 |
4 |
-0.7 |
-0.7 |
2.2 |
1.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
0 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
2.6 |
2.6 |
3.1 |
0.4 |
1.8 |
3.4 |
-0.7 |
-0.7 |
-0.7 |
3.1 |
3 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
1.1 |
-0.7 |
-0.7 |
-0.7 |
-0.6 |
-0.3 |
-0.7 |
-0.7 |
0.1 |
-0.1 |
-0.8 |
-0.7 |
0.5 |
-0.3 |
-0.7 |
-0.7 |
1.3 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.1 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
0.8 |
-0.7 |
-0.7 |
1.3 |
1.3 |
1.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
-0.7 |
At1g80820 |
261899_at |
CCR2 |
cinnamoyl CoA reductase isoform 2. Involved in lignin biosynthesis. |
10 |
cinnamoyl-CoA reductase activity | lignin biosynthesis |
|
lignin biosynthesis |
|
Phenylpropanoid Metabolism | core phenylpropanoid metabolism |
|
Phenylpropanoid pathway |
|
3.91 |
6.17 |
At3g12500 |
0.523 |
ATHCHIB |
basic endochitinase |
2.3 |
2.1 |
1.7 |
1.6 |
1.8 |
1.2 |
0.4 |
0.1 |
0 |
0.2 |
1.4 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
1.3 |
4.4 |
4.5 |
3.1 |
2.7 |
1.3 |
1.6 |
4.1 |
4.7 |
4.5 |
4.2 |
3.9 |
3.8 |
1.4 |
4.3 |
1.3 |
2.2 |
3.5 |
2.7 |
2.6 |
2.3 |
2.1 |
2 |
2.1 |
2.2 |
1.7 |
2.1 |
2.5 |
1.6 |
1.6 |
2.1 |
1.9 |
1.9 |
-1.8 |
1.2 |
3.1 |
-1.8 |
-1.8 |
-1.8 |
-0.2 |
-1.8 |
-0.3 |
3.7 |
2.7 |
5.9 |
5.8 |
-1.8 |
-1.8 |
-1.8 |
-0.2 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
1.6 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
0.7 |
0.9 |
1.5 |
-1.8 |
3.1 |
1.6 |
-1.8 |
3.5 |
4.5 |
4.2 |
1.8 |
-1.8 |
-1.8 |
4.2 |
4 |
2 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
5.1 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
1.6 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
0.1 |
1.2 |
-1.8 |
0 |
-1.8 |
0 |
-1.8 |
-0.2 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.3 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
-1.8 |
0.5 |
0.5 |
-1.8 |
-1.8 |
-1.8 |
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 |
|
|
|
|
6.18 |
7.81 |
At3g04880 |
0.522 |
DRT102 |
encodes a novel protein involved in DNA repair from UV damage. Isolated by functional complementation of E. coli UV-sensitive mutants (UVR genes). |
0.1 |
0.3 |
0.5 |
0.1 |
0.5 |
0.5 |
0.4 |
0.4 |
0.1 |
0.3 |
0.6 |
0.8 |
0.4 |
0.1 |
0.2 |
0.4 |
0 |
0 |
0.4 |
1.1 |
0.7 |
0.6 |
-0.8 |
-0.2 |
0 |
1.5 |
1.9 |
1.7 |
2 |
1.9 |
1.9 |
-0.2 |
0.3 |
-0.2 |
0 |
0.3 |
0 |
0.5 |
0 |
0.3 |
-0.1 |
0 |
0 |
0.3 |
0.1 |
0.1 |
0.1 |
0 |
0 |
0.5 |
0.3 |
-0.2 |
-0.2 |
1.4 |
0 |
0.5 |
-0.1 |
-0.2 |
0.1 |
0.3 |
0.1 |
0.1 |
0.5 |
1.9 |
-0.1 |
-0.3 |
0 |
0.5 |
0.3 |
0.1 |
-0.2 |
-0.1 |
-0.3 |
0 |
0.1 |
-0.3 |
-0.8 |
-0.9 |
-0.6 |
-0.3 |
-0.3 |
-0.3 |
-0.4 |
-0.3 |
-0.4 |
-0.3 |
0 |
0 |
-0.2 |
-0.1 |
-0.2 |
-0.1 |
0.1 |
0.3 |
1.3 |
0.5 |
0.9 |
1.3 |
-0.2 |
-0.4 |
-0.5 |
0 |
1.2 |
0.4 |
0.2 |
0.6 |
0 |
0 |
0.4 |
-0.8 |
-0.7 |
-0.5 |
-0.4 |
-0.4 |
-0.4 |
-0.3 |
-0.4 |
-0.4 |
-0.3 |
-0.4 |
-0.6 |
-0.7 |
-0.8 |
-0.6 |
-0.3 |
-0.4 |
0.1 |
0.3 |
-0.1 |
-0.3 |
-0.9 |
-0.5 |
-0.9 |
-1 |
-0.4 |
-0.4 |
-1.6 |
-0.9 |
-0.7 |
-0.6 |
-0.3 |
-2.3 |
-2.3 |
-2.3 |
-2.3 |
-2.3 |
-0.6 |
-0.2 |
-0.7 |
-0.5 |
-0.4 |
-0.1 |
-0.4 |
0.2 |
0.1 |
0.3 |
0.8 |
0.8 |
1 |
-1.3 |
0.9 |
0.9 |
1 |
1 |
0.1 |
0.3 |
-0.6 |
At3g04880 |
259100_a (m) |
DRT102 |
encodes a novel protein involved in DNA repair from UV damage. Isolated by functional complementation of E. coli UV-sensitive mutants (UVR genes). |
7 |
response to UV | photoreactive repair |
|
Calvin cycle | ribose degradation | non-oxidative branch of the pentose phosphate pathway | superpathway of gluconate degradation |
|
|
|
|
|
2.30 |
4.35 |
At1g62380 |
0.518 |
ACO2 |
Encodes a protein similar to 1-aminocyclopropane-1-carboxylic oxidase (ACC oxidase). Expression of the AtACO2 transcripts is affected by ethylene. |
1.9 |
2.1 |
2 |
2 |
2.3 |
1.8 |
1.5 |
1.1 |
1.1 |
1.3 |
2.1 |
2.1 |
1.6 |
1 |
1 |
1.2 |
1.2 |
1.3 |
1.4 |
1.2 |
1.8 |
2.1 |
2.1 |
0.7 |
0.8 |
0.4 |
0.3 |
0.7 |
0.9 |
0.6 |
0.6 |
1 |
0.6 |
1.1 |
0.5 |
1.7 |
0.3 |
0.7 |
0.5 |
0.7 |
0.5 |
0.1 |
0.1 |
0.2 |
0 |
-0.2 |
-0.6 |
-0.4 |
-0.1 |
1.5 |
1.9 |
0 |
1 |
1.5 |
0.5 |
0.1 |
0.1 |
0.9 |
0 |
-0.1 |
1.1 |
1.7 |
2 |
1 |
0.1 |
-0.1 |
0 |
0.3 |
-0.1 |
0.4 |
0.5 |
0.7 |
0.6 |
0.3 |
-0.2 |
0.8 |
0.3 |
-0.1 |
-0.5 |
0 |
-0.3 |
0 |
0 |
1 |
0.1 |
-0.3 |
0.8 |
0.1 |
0.1 |
-0.3 |
0 |
0.5 |
0.3 |
-0.5 |
0.7 |
0.1 |
-1.6 |
1.1 |
0.3 |
-1.1 |
-0.1 |
0 |
1.3 |
1.8 |
1.7 |
0.4 |
0.4 |
1.6 |
0.1 |
-0.1 |
-0.2 |
-0.9 |
-2.6 |
-2 |
-2 |
-1.5 |
-2.7 |
-2.9 |
-2.5 |
-2.2 |
-1.1 |
-1 |
-0.7 |
1.9 |
-0.1 |
2.1 |
0.8 |
0.1 |
0.4 |
1.8 |
-0.1 |
1.1 |
-0.5 |
0.6 |
-0.8 |
2.5 |
-1.5 |
2.8 |
-0.3 |
1.3 |
1.1 |
-6.1 |
-6.1 |
-6.1 |
-6.1 |
-6.1 |
-0.9 |
-0.6 |
0.4 |
0.9 |
1.1 |
1.1 |
1.2 |
0.5 |
1 |
0.7 |
-5 |
-5.1 |
-2.1 |
-6.1 |
-4.2 |
-4.8 |
0.8 |
0.8 |
-6.1 |
-6.1 |
-4 |
At1g62380 |
260637_at |
ACO2 |
Encodes a protein similar to 1-aminocyclopropane-1-carboxylic oxidase (ACC oxidase). Expression of the AtACO2 transcripts is affected by ethylene. |
6 |
detection of ethylene stimulus |
|
|
|
Biosynthesis of Amino Acids and Derivatives | Methionin/SAM/ethylene metabolism from cysteine and aspartate |
|
|
|
7.24 |
8.95 |
At1g20950 |
0.515 |
|
Similar to pyrophosphate--fructose 6-phosphate 1-phosphotransferase alpha subunit from Ricinus communis |
0 |
0.1 |
0.2 |
0.5 |
0.5 |
0.6 |
0.5 |
0.4 |
0.5 |
0.3 |
-1.2 |
1.1 |
1.5 |
1.7 |
1.2 |
1.2 |
1 |
0.6 |
0.2 |
0 |
-0.1 |
-2.7 |
-0.1 |
0.7 |
-1.2 |
1.2 |
0.9 |
0.6 |
0.7 |
0.4 |
0.7 |
0.4 |
0 |
0.4 |
0.6 |
0.8 |
0.3 |
0 |
0.2 |
0.2 |
0.5 |
0.3 |
0.2 |
-0.2 |
0.3 |
0.3 |
0.5 |
0.3 |
0.2 |
-0.9 |
-0.6 |
-0.2 |
0.8 |
-1.4 |
-0.8 |
-1.5 |
0.5 |
0.6 |
-1.4 |
-1.5 |
0.1 |
0.2 |
-0.7 |
0.7 |
0 |
-0.3 |
-0.3 |
-0.4 |
-0.5 |
-0.7 |
-0.3 |
0.1 |
0.2 |
-0.4 |
-0.2 |
0.2 |
0.8 |
0.3 |
0.5 |
0.1 |
0.1 |
0.7 |
0.6 |
0.4 |
-0.1 |
-0.3 |
-1 |
-1 |
-1.2 |
-0.9 |
-0.6 |
1.7 |
0.3 |
-2 |
1.2 |
1.1 |
-0.6 |
1.1 |
-0.8 |
-0.6 |
1.5 |
1.4 |
1.2 |
0.2 |
0.9 |
0.2 |
0.4 |
1 |
-1.1 |
1.1 |
1.3 |
1.4 |
0.9 |
1.1 |
1 |
1 |
1.2 |
1.2 |
1.3 |
1.2 |
1.1 |
0.6 |
0.6 |
-0.4 |
0.2 |
0.2 |
0.7 |
-0.6 |
-0.3 |
0.1 |
0.6 |
0.3 |
-0.7 |
-2.1 |
1.1 |
-2.5 |
-0.2 |
-2.4 |
1 |
0.7 |
0.8 |
-1.3 |
-2.1 |
-2 |
-2 |
-2 |
-0.1 |
-0.7 |
0.4 |
0.8 |
0.7 |
0.3 |
-0.3 |
-2.4 |
-2 |
-2 |
-2.4 |
-3 |
-1.1 |
0.5 |
-2.9 |
-3.2 |
-0.2 |
-0.2 |
0.1 |
-0.7 |
0.4 |
At1g20950 |
262806_at |
|
Similar to pyrophosphate--fructose 6-phosphate 1-phosphotransferase alpha subunit from Ricinus communis |
4 |
|
C-compound and carbohydrate metabolism | glycolysis and gluconeogenesis |
mannitol degradation | sorbitol fermentation | sorbitol degradation | fructose degradation (anaerobic) | acetate fermentation | glycolysis I | glycolysis IV |
Fructose and mannose metabolism |
Intermediary Carbon Metabolism |
|
|
|
3.43 |
4.99 |
At5g66120 |
0.515 |
|
3-dehydroquinate synthase, putative, similar to aroB (Neisseria gonorrhoeae) |
0.4 |
1.2 |
1.3 |
0.5 |
0.6 |
0.5 |
0.5 |
0.4 |
0.5 |
0.2 |
0.2 |
1.2 |
0.9 |
0.5 |
0.2 |
-0.1 |
-0.6 |
0 |
-0.5 |
0.4 |
0 |
0 |
1.4 |
0.5 |
-0.4 |
0.4 |
0 |
0 |
0.1 |
0 |
0.1 |
0.2 |
-0.1 |
0.1 |
0.1 |
0.1 |
-0.2 |
-0.3 |
-0.2 |
-0.2 |
0 |
0 |
-0.2 |
-0.3 |
-0.2 |
-0.1 |
-0.2 |
-0.1 |
-0.1 |
0 |
-0.4 |
0.3 |
0 |
-0.1 |
0.5 |
0 |
0.6 |
0.9 |
0.1 |
0 |
1 |
0.9 |
1.2 |
0.6 |
0.2 |
0.3 |
0 |
0.2 |
0.2 |
0 |
0 |
0.1 |
0.3 |
0.2 |
0.2 |
0.3 |
0.6 |
0.4 |
0.5 |
0.3 |
0.2 |
0.5 |
0.3 |
0.3 |
0.5 |
0.3 |
0 |
0.2 |
0.2 |
0.2 |
0 |
0 |
-1.2 |
-2.3 |
0.2 |
0.3 |
-0.3 |
0.8 |
-0.9 |
-1 |
0.8 |
0.7 |
0.8 |
-0.8 |
0.5 |
0.3 |
-0.1 |
0.1 |
0.1 |
-0.2 |
-0.3 |
-0.5 |
-0.6 |
-0.6 |
-0.7 |
-0.6 |
-0.6 |
-0.5 |
-0.6 |
-0.6 |
-0.1 |
0 |
0 |
0.1 |
0 |
0.2 |
0 |
-0.2 |
0.1 |
-1.2 |
-0.1 |
0 |
0.5 |
0.7 |
0.3 |
0.2 |
0 |
0.1 |
-0.4 |
-0.3 |
0 |
-1.6 |
-1.1 |
-2.7 |
-2.5 |
-2.3 |
0.6 |
0.4 |
0 |
0.3 |
0.2 |
0.2 |
0.3 |
0 |
0.2 |
0 |
-1.1 |
-0.8 |
-0.4 |
-0.1 |
-0.8 |
0 |
-0.9 |
-0.9 |
0 |
0 |
-0.4 |
At5g66120 |
247138_at |
|
3-dehydroquinate synthase, putative, similar to aroB (Neisseria gonorrhoeae) |
4 |
|
|
chorismate biosynthesis |
Phenylalanine, tyrosine and tryptophan biosynthesis |
Phenylpropanoid Metabolism | Aromatic amino acid (Phe, Tyr, Trp) metabolism |
|
Shikimate pathway | chorismate biosynthesis |
|
1.99 |
4.23 |
At3g43190 |
0.514 |
|
strong similarity to Sucrose synthase (Arabidopsis thaliana) (SUS1) |
4.3 |
3.3 |
1.6 |
0.9 |
1.2 |
1.6 |
1.9 |
2.4 |
0.2 |
-0.5 |
-0.7 |
-0.1 |
-0.7 |
-1.4 |
-0.8 |
-0.9 |
-1 |
-1.2 |
4.4 |
3.7 |
3.7 |
1.8 |
0.2 |
-0.6 |
-1 |
5.6 |
5.9 |
6 |
5.8 |
5.9 |
5.8 |
-0.2 |
4.2 |
-1.1 |
0.7 |
2.2 |
0.7 |
1 |
0.1 |
0.1 |
0.5 |
0.7 |
1.2 |
0 |
0.2 |
0.5 |
0.3 |
0.1 |
0.2 |
0.1 |
-0.9 |
-1.3 |
-0.1 |
0 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.1 |
-1.3 |
1.3 |
4.6 |
-1.3 |
-1.3 |
-1.2 |
-1.2 |
-1.3 |
-1.3 |
-1.1 |
-1.2 |
-1.2 |
-1.3 |
-1.3 |
-0.2 |
-0.5 |
-0.6 |
-0.6 |
-1 |
-0.5 |
-1 |
-0.9 |
-0.6 |
-1.2 |
-1.3 |
-0.6 |
-0.9 |
-1.3 |
-1.3 |
-1.3 |
0.9 |
6 |
6.2 |
3 |
2.5 |
2.2 |
2.4 |
-1.3 |
-1.3 |
0.9 |
0.9 |
2.6 |
-0.9 |
-0.2 |
1 |
-1.1 |
1.3 |
-0.2 |
-1.5 |
-0.9 |
-0.7 |
-0.7 |
-1.5 |
-0.7 |
-1.8 |
0.9 |
1.1 |
0.4 |
-1.5 |
-1.6 |
-1.3 |
-1.3 |
-1.4 |
-1.3 |
-1.3 |
-0.5 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.2 |
-1.4 |
-1.1 |
-1.4 |
-1.2 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
0.5 |
0.2 |
0.5 |
0.6 |
0.2 |
-0.3 |
-1 |
-1.3 |
-1.3 |
-1.3 |
-1.3 |
-1.5 |
-0.5 |
-1.3 |
-1.3 |
-1.3 |
-0.6 |
-0.6 |
-1.3 |
-1.3 |
-2.1 |
At3g43190 |
252746_at |
|
strong similarity to Sucrose synthase (Arabidopsis thaliana) (SUS1) |
6 |
|
C-compound, carbohydrate anabolism | glycolysis and gluconeogenesis |
sucrose biosynthesis | sucrose degradation III |
Starch and sucrose metabolism |
Cell Wall Carbohydrate Metabolism | sucrose metabolism |
|
|
|
6.08 |
8.34 |
At3g20960 |
0.510 |
CYP705A33 |
cytochrome P450 family protein |
1.6 |
2.5 |
0.8 |
0.9 |
1.1 |
0.9 |
0.1 |
0.1 |
1 |
0 |
1.4 |
1.7 |
1.3 |
0 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0.6 |
0.5 |
0 |
-0.5 |
-1.3 |
0 |
0.7 |
0.7 |
0.7 |
0.2 |
0.8 |
0.9 |
1 |
0.7 |
0 |
-0.5 |
0.1 |
0.8 |
1.1 |
1 |
0.8 |
0.7 |
0.8 |
0.6 |
0.6 |
1.1 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
1.2 |
1 |
-0.5 |
-0.2 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0.3 |
0.5 |
1.5 |
1.3 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0.2 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0.4 |
1.1 |
1 |
1.3 |
-0.5 |
1.3 |
1.2 |
0.6 |
2.3 |
2.5 |
2.1 |
2 |
-0.5 |
-0.5 |
1.9 |
2.1 |
2 |
-0.5 |
-0.2 |
-0.5 |
-0.5 |
0.4 |
0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.3 |
-0.6 |
-0.5 |
-1 |
-1.2 |
-1 |
-0.5 |
-0.5 |
-0.9 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.6 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0.6 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
-0.5 |
0 |
0 |
-0.5 |
-0.5 |
-0.5 |
At3g20960 |
256803_at |
CYP705A33 |
cytochrome P450 family protein |
1 |
|
|
|
|
|
|
|
cytochrome P450 family |
2.25 |
3.89 |
At4g30190 |
0.510 |
AHA2 |
belongs to the P-type ATPase superfamily of cation-transporting ATPases, pumps protons out of the cell, generating a proton gradient that drives the active transport of nutrients by proton symport. |
-0.4 |
2 |
0.5 |
0 |
0.7 |
0.8 |
0.9 |
0.5 |
0.5 |
0.7 |
0.3 |
2 |
1.3 |
1.3 |
1.2 |
1 |
0.9 |
0.5 |
0.6 |
0.7 |
0.7 |
-0.3 |
1.4 |
0 |
-1.7 |
0.3 |
0.2 |
0.4 |
0.4 |
0.3 |
0.5 |
0.5 |
0.9 |
-0.5 |
1 |
0.8 |
1.1 |
1.2 |
1 |
1.2 |
1.3 |
1.2 |
1.2 |
1.1 |
1.2 |
1.2 |
1.2 |
1.1 |
0.7 |
0 |
0.4 |
-0.3 |
-0.1 |
-0.7 |
-1.4 |
-1.1 |
1.6 |
1.8 |
-1 |
-1 |
1.4 |
1.2 |
1.8 |
1.2 |
0.5 |
-0.1 |
0.1 |
0.5 |
0.4 |
0.1 |
0 |
0 |
0 |
0 |
0.4 |
0.5 |
-0.5 |
-0.2 |
0.1 |
0.1 |
0.1 |
-0.4 |
-0.5 |
0.2 |
-0.1 |
-0.4 |
-0.8 |
0.2 |
0.4 |
0.6 |
-0.4 |
1.3 |
0.7 |
-0.5 |
1.8 |
1.1 |
1.5 |
1.7 |
-1.5 |
-1.9 |
1.6 |
1.5 |
1.7 |
-0.2 |
-1.1 |
-1.8 |
0.2 |
0.4 |
-1.9 |
-0.8 |
-0.7 |
-2.2 |
-0.9 |
-1.1 |
-1.7 |
-2 |
-0.2 |
-0.8 |
-1 |
-1.3 |
-1.2 |
-0.7 |
-0.5 |
0.4 |
-0.2 |
0.1 |
-0.3 |
-0.9 |
-0.4 |
0 |
-0.9 |
-0.7 |
-0.3 |
1.1 |
0.1 |
1.2 |
-0.2 |
1 |
-1.2 |
-0.8 |
0.4 |
-2.8 |
-2.1 |
-2.8 |
-2.8 |
-2.8 |
-1 |
-1 |
-1.4 |
-0.6 |
-0.8 |
-0.3 |
-0.4 |
-1.2 |
-1.1 |
-1.2 |
-3 |
-3.1 |
-1 |
1 |
-3.3 |
-1.1 |
1 |
1 |
0.5 |
0.3 |
0.7 |
At4g30190 |
253609_at |
AHA2 |
belongs to the P-type ATPase superfamily of cation-transporting ATPases, pumps protons out of the cell, generating a proton gradient that drives the active transport of nutrients by proton symport. |
9 |
hydrogen-exporting ATPase activity, phosphorylative mechanism | nutrient import |
transport facilitation | transport ATPases | eukaryotic plasma membrane / membrane attached |
|
Oxidative phosphorylation |
|
|
|
|
3.72 |
5.36 |
At2g17720 |
0.509 |
|
oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to prolyl 4-hydroxylase, alpha subunit, from Gallus gallus, Rattus norvegicus, Mus musculus |
2.7 |
3.4 |
2.2 |
1.4 |
2.1 |
2.8 |
3.4 |
3.2 |
3.5 |
3.8 |
3.5 |
2.2 |
2.2 |
2.6 |
2.5 |
2.3 |
1.4 |
3.6 |
2.3 |
1.7 |
0.4 |
-1.1 |
-1.1 |
-0.1 |
-0.6 |
0 |
2 |
1.9 |
-0.7 |
-0.6 |
-1.4 |
-0.1 |
-0.9 |
-0.4 |
-0.6 |
0 |
-0.1 |
0 |
-0.2 |
0 |
-0.2 |
-0.3 |
-1.1 |
-0.2 |
-0.4 |
-1.1 |
-1.1 |
-1.1 |
-1.1 |
-1.1 |
-0.4 |
0 |
0.7 |
-1.1 |
0.1 |
0.3 |
0 |
-0.2 |
0.2 |
0.4 |
-0.1 |
-0.3 |
-1.1 |
-0.5 |
0.2 |
0.1 |
0 |
0.2 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.4 |
0.3 |
0.5 |
0.4 |
0 |
-0.5 |
-0.3 |
0 |
0.5 |
0.6 |
-0.1 |
-0.1 |
0 |
0.8 |
0.1 |
0.3 |
0 |
0.1 |
0.8 |
-0.3 |
1.4 |
0.3 |
0.5 |
1 |
0 |
0.1 |
-0.4 |
0 |
-0.1 |
0.1 |
-0.8 |
0 |
0.7 |
-0.7 |
0.7 |
0.4 |
-0.6 |
-0.6 |
-1 |
0 |
-0.3 |
-0.9 |
-0.8 |
0.3 |
0 |
-0.6 |
-1.1 |
-1.1 |
-0.7 |
-1.1 |
-0.7 |
-0.8 |
-1.1 |
-0.7 |
-0.5 |
-0.9 |
-0.8 |
-1 |
-0.6 |
-0.7 |
-0.3 |
-1.2 |
-1.3 |
-1.5 |
-1.1 |
-1.2 |
-1.2 |
-0.3 |
-0.1 |
-0.8 |
-1.1 |
-1.1 |
-1.1 |
-0.1 |
0.5 |
-1.3 |
-1.3 |
-1.2 |
-1.5 |
-1.5 |
-1.2 |
-0.8 |
-0.9 |
-1.2 |
-1.7 |
-0.4 |
-0.8 |
-2 |
0.3 |
-1.2 |
-1.2 |
0 |
-0.1 |
-1 |
At2g17720 |
264592_at |
|
oxidoreductase, 2OG-Fe(II) oxygenase family protein, similar to prolyl 4-hydroxylase, alpha subunit, from Gallus gallus, Rattus norvegicus, Mus musculus |
2 |
|
|
|
|
Biosynthesis of Amino Acids and Derivatives | Prolin/Hydroxyproline from glutamate |
|
|
|
4.06 |
5.89 |
At3g43600 |
0.508 |
AAO2 |
aldehyde oxidase, putative |
0.4 |
-0.3 |
0.4 |
0.9 |
0.3 |
0.4 |
0.2 |
0.4 |
0 |
-0.1 |
1.6 |
2 |
2 |
2 |
1.1 |
1.4 |
0.9 |
0.8 |
0.7 |
1.1 |
0.6 |
0 |
1.8 |
1.4 |
0.5 |
1.8 |
1.3 |
1.7 |
1.3 |
1.5 |
1.2 |
0.6 |
1 |
0.7 |
0.9 |
1.3 |
0.8 |
0.7 |
0.8 |
1 |
1.1 |
1 |
0.9 |
0.9 |
0.8 |
0.7 |
1 |
0.9 |
0.4 |
1.3 |
1.7 |
0.4 |
2 |
-0.9 |
-0.9 |
-0.7 |
0 |
0 |
-0.9 |
-0.9 |
0.5 |
0.8 |
1.3 |
1.4 |
-0.1 |
-0.3 |
-0.5 |
-0.7 |
-0.6 |
-0.7 |
-0.6 |
-0.2 |
-0.5 |
-0.2 |
0 |
0.4 |
0.4 |
0.1 |
0 |
-0.1 |
0 |
-0.5 |
-0.5 |
0.1 |
-0.5 |
-1.2 |
0.6 |
0 |
-0.2 |
0.7 |
-1.2 |
1 |
-0.9 |
-0.9 |
0.8 |
0.8 |
1.8 |
0.9 |
-0.9 |
-0.9 |
0.8 |
1.1 |
1 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-1.3 |
-0.9 |
0.4 |
0.8 |
-0.3 |
0.2 |
-0.4 |
-0.3 |
-0.5 |
0.3 |
-0.4 |
-0.6 |
-1.3 |
-0.9 |
-0.9 |
-1.5 |
-0.9 |
-0.9 |
-0.9 |
-1.2 |
-0.9 |
-0.9 |
-0.9 |
-1.3 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-1 |
-0.9 |
-0.9 |
-0.9 |
-0.8 |
-0.9 |
0.1 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-0.9 |
-1 |
-0.6 |
-0.2 |
-0.5 |
-0.9 |
-0.9 |
-0.9 |
-1.3 |
-1.2 |
-0.8 |
0.3 |
-1.8 |
-1.4 |
-0.1 |
-0.1 |
-0.6 |
-1 |
0.4 |
At3g43600 |
246330_at |
AAO2 |
aldehyde oxidase, putative |
9 |
aldehyde oxidase activity | abscisic acid biosynthesis |
metabolism |
|
|
|
|
|
|
2.95 |
3.90 |
At3g21770 |
0.507 |
|
peroxidase 30 (PER30) (P30) (PRXR9) |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
0.8 |
0.9 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
0.8 |
0.2 |
-1.4 |
-0.9 |
0.9 |
0 |
2.7 |
2.4 |
2.8 |
2.3 |
1.3 |
1.6 |
1.1 |
3 |
0.7 |
1.1 |
2.8 |
1.9 |
1.9 |
2.1 |
1.7 |
1.7 |
2.1 |
2.4 |
1.9 |
1.4 |
1.9 |
2 |
1.6 |
2.2 |
1.5 |
1.8 |
-1.4 |
4.1 |
0.9 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-0.4 |
1.1 |
2.6 |
-1.4 |
-1.4 |
-1.4 |
-0.9 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
2.5 |
-0.4 |
0 |
-0.1 |
0.3 |
0.1 |
-1.4 |
-1.4 |
-0.3 |
-1.4 |
-1.3 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
4.6 |
3.2 |
2.4 |
4 |
4.2 |
3.9 |
4 |
-1.4 |
-1.4 |
3.7 |
3.3 |
4.1 |
-1.4 |
-1 |
0.6 |
0.6 |
1.3 |
-1.4 |
0.5 |
1.4 |
0.8 |
1.8 |
2 |
1.8 |
1.9 |
0.7 |
1.2 |
0.6 |
-0.9 |
-0.5 |
-0.6 |
-1 |
0 |
-0.4 |
-1.1 |
-0.3 |
-0.8 |
0 |
0.6 |
-0.1 |
-1.4 |
-1.4 |
-1.1 |
-1.4 |
-1 |
-0.5 |
-0.2 |
-1.1 |
0 |
-0.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
0 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-1.4 |
-0.3 |
-0.3 |
-1.4 |
-1.4 |
-1.4 |
At3g21770 |
257952_at |
|
peroxidase 30 (PER30) (P30) (PRXR9) |
2 |
|
|
|
Methane metabolism | Prostaglandin and leukotriene metabolism | Phenylalanine metabolism | Stilbene, coumarine and lignin biosynthesis |
|
|
|
Glycosyl transferase, Family 1 |
4.75 |
6.08 |
At1g30510 |
0.504 |
|
Strong similarity to Ferredoxin--NADP reductase chloroplast precursorfrom Oryza sativa and Zea mays |
0.6 |
0.7 |
0.6 |
0.6 |
0.3 |
0.5 |
0.7 |
0.3 |
0.2 |
0 |
-1 |
2.1 |
2.3 |
1.1 |
0.4 |
0.4 |
0.6 |
0.6 |
0.6 |
0 |
-0.1 |
-1.7 |
1.7 |
1.6 |
-0.6 |
0.9 |
0.4 |
0.3 |
1.1 |
0.7 |
0.6 |
0.2 |
0.3 |
-0.9 |
1.1 |
1 |
1.5 |
1.8 |
2 |
2 |
1.8 |
2.2 |
2.1 |
2.2 |
2.3 |
1.8 |
2 |
2.2 |
2 |
-1.5 |
-0.5 |
-0.6 |
1.6 |
0.1 |
-1.8 |
-1.9 |
-1.6 |
-0.9 |
-2 |
-2.2 |
-0.8 |
-0.4 |
-0.6 |
0.3 |
-0.4 |
-0.4 |
-1 |
-0.5 |
-1 |
-1.9 |
-1.4 |
-1.1 |
-0.7 |
-0.8 |
-0.7 |
-0.3 |
0 |
-0.4 |
-0.6 |
-0.3 |
-0.3 |
-1.1 |
-1 |
0.6 |
-0.2 |
-0.8 |
-0.5 |
-0.8 |
-1 |
-0.4 |
-1.3 |
2.8 |
0.8 |
-0.7 |
3.6 |
3.2 |
1.7 |
3.3 |
-1.4 |
-1 |
2.3 |
2.2 |
3.5 |
0 |
0 |
0.5 |
-0.3 |
1.2 |
-0.3 |
-0.4 |
0 |
-0.2 |
0.6 |
0.5 |
0.1 |
0.3 |
0.6 |
0 |
0 |
-0.1 |
-0.3 |
-0.4 |
-0.7 |
-0.6 |
-0.5 |
-0.6 |
0.1 |
-0.5 |
-0.5 |
-0.1 |
-0.5 |
0 |
-1.1 |
-1.1 |
0 |
-1 |
-1.4 |
-0.7 |
-0.4 |
-0.1 |
-0.4 |
0.4 |
0.7 |
-1.7 |
-1.7 |
-1.7 |
0.4 |
0 |
0 |
0.4 |
0.2 |
0 |
-0.3 |
-1.7 |
-1.7 |
-1.7 |
-2 |
-2.3 |
-1 |
0 |
-2.2 |
-0.2 |
-1.7 |
-1.7 |
-2 |
-1.9 |
-0.5 |
At1g30510 |
261806_at |
|
Strong similarity to Ferredoxin--NADP reductase chloroplast precursorfrom Oryza sativa and Zea mays |
6 |
|
|
|
Photosynthesis |
Photosystems | Ferredoxin |
|
|
|
4.16 |
6.00 |