EC Number |
Recommended Name |
Source Tissue |
Reference |
---|
1.1.1.183 | geraniol dehydrogenase (NADP+) |
stem |
- |
741134 |
1.1.1.194 | coniferyl-alcohol dehydrogenase |
stem |
- |
760935 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
- |
-, 656926, 657055, 700730, 739876, 740176, 740239, 740539, 741132, 741181, 760238, 760990, 761954 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
constitutively expressed |
725940 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
elongating |
670637 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
FC1 is expressed slightly more at the seedling stage than at the heading stage. At the heading stage, a strong FC1 expression level in the first internode |
700777 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
high expression |
712611 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
highest CAD2 expression level in stems |
740176 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
highest expression of isoform CAD4 |
761743 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
highly expressed in developing stem. Of the seven CAD genes identified in Brachypodium distachyon, BdCAD1 expression is greatest in stem tissue, exhibiting 10fold higher transcript level than any of the other seven BdCAD genes |
733569 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
internode |
700841 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
isoforms Cad-4, Cad-5, Cad-7, Cad-8, expression in lignifying stem tissue. No expression of isoforms Cad-2, Cad-3 in lignifying tissue |
689419 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
low expression of CAD3 in stem |
741132 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
mature stem |
347822 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
mRNA is more abundant in the lower stem than in the upper stem |
686987 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
transcriptional patterns of TaCAD12 in wheat stems after Rhizoctonia cerealis inoculation analyzed by quantitative RT-PCR, overview |
738304 |
1.1.1.195 | cinnamyl-alcohol dehydrogenase |
stem |
young section |
347811, 347813 |
1.1.1.200 | aldose-6-phosphate reductase (NADPH) |
stem |
- |
761738 |
1.1.1.206 | tropinone reductase I |
stem |
- |
740901, 740981, 741124, 760748 |
1.1.1.206 | tropinone reductase I |
stem |
high enzyme level in bark, moderate in medulla |
741278 |
1.1.1.206 | tropinone reductase I |
stem |
low expression level |
760748 |
1.1.1.206 | tropinone reductase I |
stem |
transcript level of TRI is low |
696874 |
1.1.1.219 | dihydroflavonol 4-reductase |
stem |
- |
669664, 740507, 741277, 741282 |
1.1.1.219 | dihydroflavonol 4-reductase |
stem |
high expression level in lower stem |
760791 |
1.1.1.219 | dihydroflavonol 4-reductase |
stem |
weak expression |
740507 |
1.1.1.22 | UDP-glucose 6-dehydrogenase |
stem |
- |
654351, 740128 |
1.1.1.22 | UDP-glucose 6-dehydrogenase |
stem |
identification of nine putative UGDH genes, more than 77% of the genes are predominantly expressed in the stem |
762397 |
1.1.1.236 | tropinone reductase II |
stem |
- |
348025, 348033, 740901, 760748 |
1.1.1.236 | tropinone reductase II |
stem |
about half of the expression in root |
760748 |
1.1.1.236 | tropinone reductase II |
stem |
transcript level of TRII is high |
696874 |
1.1.1.237 | hydroxyphenylpyruvate reductase |
stem |
- |
-, 700368, 739871, 741318, 761180 |
1.1.1.24 | quinate/shikimate dehydrogenase (NAD+) |
stem |
lowest expression level |
762187 |
1.1.1.247 | codeinone reductase (NADPH) |
stem |
high expression in upper stem. Peaks of expression are at flowering and lancing |
740521 |
1.1.1.247 | codeinone reductase (NADPH) |
stem |
localized in laticifers |
657166 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
stem |
- |
761171 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
stem |
highest expression level |
762187 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
stem |
lowest expression level |
762187 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
- |
690214, 695411, 720429, 762525 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
DXR is most actively transcribed in the stem wood |
701348 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
high expression level |
741146 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
in seedling, higher expression in stem and leaf than in root |
688649 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
moderate expression level |
676660 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
sapwood and heartwood |
763120 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
strong expression |
740825 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
strong expression of mRNA |
688641 |
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
stem |
upper and lower parts |
763591 |
1.1.1.282 | quinate/shikimate dehydrogenase [NAD(P)+] |
stem |
green |
762145 |
1.1.1.282 | quinate/shikimate dehydrogenase [NAD(P)+] |
stem |
Poptr3 is highly expressed in bark and some vascular tissues |
740724 |
1.1.1.284 | S-(hydroxymethyl)glutathione dehydrogenase |
stem |
- |
-, 724489, 763592, 763605 |
1.1.1.294 | chlorophyll(ide) b reductase |
stem |
- |
763632 |
1.1.1.294 | chlorophyll(ide) b reductase |
stem |
low expression level |
762974 |
1.1.1.316 | L-galactose 1-dehydrogenase |
stem |
- |
713254 |
1.1.1.324 | 8-hydroxygeraniol dehydrogenase |
stem |
low expression level |
763575 |
1.1.1.326 | zerumbone synthase |
stem |
- |
717593 |
1.1.1.330 | very-long-chain 3-oxoacyl-CoA reductase |
stem |
gene KCR3 transcripts accumulate in rapidly elongating fibers, roots and stem |
718814 |
1.1.1.330 | very-long-chain 3-oxoacyl-CoA reductase |
stem |
inflorescence stem |
700827 |
1.1.1.330 | very-long-chain 3-oxoacyl-CoA reductase |
stem |
low expression |
719240 |
1.1.1.331 | secoisolariciresinol dehydrogenase |
stem |
- |
743768 |
1.1.1.334 | methylecgonone reductase |
stem |
less than 20% of activity compared to young leaves |
718331 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
stem |
- |
740956, 740983, 760804, 761172, 761343, 762456 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
stem |
lower |
740956 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
stem |
strong expression |
668026 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
stem |
weak expression |
700117 |
1.1.1.37 | malate dehydrogenase |
stem |
- |
654907, 762119, 762120 |
1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
stem |
- |
689506, 697065, 739251 |
1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
stem |
expression of NADP-ME3 is restricted to the trichomes and trichome basal cells of leaves and stems |
670594 |
1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
stem |
isozymes S1 and S2 |
686932 |
1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
stem |
lighified |
723150 |
1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
stem |
NADP-ME4 |
670594 |
1.1.1.41 | isocitrate dehydrogenase (NAD+) |
stem |
- |
-, 657111, 670547 |
1.1.1.415 | noscapine synthase |
stem |
NOS transcripts are detected in all opium poppy organs, but are most abundant in stems |
748942 |
1.1.1.42 | isocitrate dehydrogenase (NADP+) |
stem |
- |
762498 |
1.1.1.42 | isocitrate dehydrogenase (NADP+) |
stem |
low expression level |
-, 722338 |
1.1.1.44 | phosphogluconate dehydrogenase (NADP+-dependent, decarboxylating) |
stem |
- |
741438 |
1.1.1.81 | hydroxypyruvate reductase |
stem |
- |
-, 761180 |
1.1.1.81 | hydroxypyruvate reductase |
stem |
moderate expression level |
-, 763559 |
1.1.1.85 | 3-isopropylmalate dehydrogenase |
stem |
- |
668015 |
1.1.3.15 | (S)-2-hydroxy-acid oxidase |
stem |
- |
762869 |
1.1.3.15 | (S)-2-hydroxy-acid oxidase |
stem |
moderate expression level |
762869 |
1.1.3.9 | galactose oxidase |
stem |
- |
763570 |
1.10.3.1 | catechol oxidase |
stem |
- |
673775, 673779, 676649 |
1.10.3.3 | L-ascorbate oxidase |
stem |
- |
439908, 657108, 742708 |
1.10.3.3 | L-ascorbate oxidase |
stem |
broccoli stalks show lower AAO activity compared to florets |
712620 |
1.11.1.11 | L-ascorbate peroxidase |
stem |
- |
688913, 700220 |
1.11.1.11 | L-ascorbate peroxidase |
stem |
activity decreases during germination, strongly increases during callus induction and proliferation, and decreases during shoot and root induction |
741633 |
1.11.1.11 | L-ascorbate peroxidase |
stem |
expression levels are higher in leaves than in roots or stems |
743788 |
1.11.1.11 | L-ascorbate peroxidase |
stem |
high expression level |
743463 |
1.11.1.11 | L-ascorbate peroxidase |
stem |
lowest expression level |
742620 |
1.11.1.13 | manganese peroxidase |
stem |
- |
725123 |
1.11.1.24 | thioredoxin-dependent peroxiredoxin |
stem |
- |
676508 |
1.11.1.7 | peroxidase |
stem |
- |
658958, 698420, 699269, 763931 |
1.11.2.3 | plant seed peroxygenase |
stem |
expression in root, stem, leaf and flower |
724973 |
1.11.2.3 | plant seed peroxygenase |
stem |
isoform Clo-3 |
713295 |
1.13.11.27 | 4-hydroxyphenylpyruvate dioxygenase |
stem |
- |
705631 |
1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
stem |
- |
673279, 673858, 742038, 764795, 765616 |
1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
stem |
abundant expression |
743160 |
1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
stem |
the VuNCED1 transcript is strongly induced in stems and leaves by drought treatment, but less in roots |
660212 |
1.13.11.53 | acireductone dioxygenase (Ni2+-requiring) |
stem |
- |
700713 |
1.13.11.54 | acireductone dioxygenase [iron(II)-requiring] |
stem |
- |
764775 |
1.13.11.58 | linoleate 9S-lipoxygenase |
stem |
low expression level |
743426 |