Basic Information
Gene Structure
Domain
Regulation&
Interaction
Annotation
Orthologus Group
Expresssion
Pathway
Basic Information
Gene ID
JreChr13G11154
View in Genome Browser
Position
chr13:2665115-2666542 (+)
1427bp
Gene Type
gene
Gene Description (Protein Product)
Belongs to the UDP-glycosyltransferase family
Organism
Juglans regia
Also AS AT4G01070

Gene Structure

upstream:
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Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
JreChr14G11003 Belongs to the peroxidase family. Classical plant (class III) peroxidase subfamily
JreChr15G11746 Belongs to the peroxidase family. Classical plant (class III) peroxidase subfamily
JreChr16G11146 Belongs to the peroxidase family. Classical plant (class III) peroxidase subfamily
Regulatory gene
JreChr01G10083 transcription factor
JreChr01G10089 dof zinc finger protein
JreChr01G10124 Homeobox-leucine zipper protein

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail

Expression Profile
DataSet Number of Samples expressed(TPM>1) Mean Min Max Standard deviation(SD) Coeffcient variation(CV)


Pathway
Go Pathway KEGG Pathway
GO Term Description GO Category
GO:0003674 molecular_function MF
GO:0003824 catalytic activity MF
GO:0005575 cellular_component CC
GO:0005622 intracellular anatomical structure CC
GO:0005623 obsolete cell CC
GO:0005737 cytoplasm CC
GO:0005783 endoplasmic reticulum CC
GO:0006725 cellular aromatic compound metabolic process BP
GO:0006805 xenobiotic metabolic process BP
GO:0006950 response to stress BP
GO:0006970 response to osmotic stress BP
GO:0008150 biological_process BP
GO:0008152 metabolic process BP
GO:0008194 UDP-glycosyltransferase activity MF
GO:0009056 catabolic process BP
GO:0009058 biosynthetic process BP
GO:0009410 response to xenobiotic stimulus BP
GO:0009628 response to abiotic stimulus BP
GO:0009636 response to toxic substance BP
GO:0009651 response to salt stress BP
GO:0009698 phenylpropanoid metabolic process BP
GO:0009699 phenylpropanoid biosynthetic process BP
GO:0009808 lignin metabolic process BP
GO:0009809 lignin biosynthetic process BP
GO:0009987 cellular process BP
GO:0012505 endomembrane system CC
GO:0016740 transferase activity MF
GO:0016757 glycosyltransferase activity MF
GO:0016758 hexosyltransferase activity MF
GO:0019438 aromatic compound biosynthetic process BP
GO:0019748 secondary metabolic process BP
GO:0035251 UDP-glucosyltransferase activity MF
GO:0042178 xenobiotic catabolic process BP
GO:0042221 response to chemical BP
GO:0043226 organelle CC
GO:0043227 membrane-bounded organelle CC
GO:0043229 intracellular organelle CC
GO:0043231 intracellular membrane-bounded organelle CC
GO:0044237 cellular metabolic process BP
GO:0044248 cellular catabolic process BP
GO:0044249 cellular biosynthetic process BP
GO:0044424 obsolete intracellular part CC
GO:0044444 obsolete cytoplasmic part CC
GO:0044464 obsolete cell part CC
GO:0044550 secondary metabolite biosynthetic process BP
GO:0046527 glucosyltransferase activity MF
GO:0050896 response to stimulus BP
GO:0051716 cellular response to stimulus BP
GO:0070887 cellular response to chemical stimulus BP
GO:0071466 cellular response to xenobiotic stimulus BP
GO:0071704 organic substance metabolic process BP
GO:0080043 quercetin 3-O-glucosyltransferase activity MF
GO:0080044 quercetin 7-O-glucosyltransferase activity MF
GO:1901360 organic cyclic compound metabolic process BP
GO:1901362 organic cyclic compound biosynthetic process BP
GO:1901576 organic substance biosynthetic process BP
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map00940 Phenylpropanoid biosynthesis Phenylpropanoids are a group of plant secondary metabolites derived from phenylalanine and having a wide variety of functions both as structural and signaling molecules. Phenylalanine is first converted to cinnamic acid by deamination. It is followed by hydroxylation and frequent methylation to generate coumaric acid and other acids with a phenylpropane (C6-C3) unit. Reduction of the CoA-activated carboxyl groups of these acids results in the corresponding aldehydes and alcohols. The alcohols are called monolignols, the starting compounds for biosynthesis of lignin.