PPGR - Gene Detail

Gene ID	CSS0030176.g View in Genome Browser
Position	Chr15:95611064-95621741 (+) 10677bp
Gene Type	gene
Gene Description (Protein Product)	Belongs to the cytochrome P450 family
Organism	Camellia sinensis
Also AS	AT5G07990

upstream:

Database	EntryID	E-Value	Start	end	InterPro ID	Description

Protein-protein interaction (PPI)	CSS0048106.g Belongs to the cytochrome P450 family CSS0046529.g Belongs to the iron ascorbate-dependent oxidoreductase family CSS0033075.g Belongs to the iron ascorbate-dependent oxidoreductase family
Regulatory gene	CSS0001631.g transcription factor CSS0001972.g transcription factor CSS0002189.g transcription factor

Load All Networks

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

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

Select Expression

GO Term	Description	GO Category
GO:0003674	molecular_function	MF
GO:0003824	catalytic activity	MF
GO:0004497	monooxygenase activity	MF
GO:0005575	cellular_component	CC
GO:0008150	biological_process	BP
GO:0008152	metabolic process	BP
GO:0009058	biosynthetic process	BP
GO:0009719	response to endogenous stimulus	BP
GO:0009725	response to hormone	BP
GO:0009733	response to auxin	BP
GO:0010033	response to organic substance	BP
GO:0016020	membrane	CC
GO:0016491	oxidoreductase activity	MF
GO:0016705	oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen	MF
GO:0016709	oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen	MF
GO:0019748	secondary metabolic process	BP
GO:0042221	response to chemical	BP
GO:0044550	secondary metabolite biosynthetic process	BP
GO:0050896	response to stimulus	BP
GO:0055114	obsolete oxidation-reduction process	BP

KEGG Term	Name	Description
map01110	Biosynthesis of secondary metabolites	-
map01100	Metabolic pathways	-
map00944	Flavone and flavonol biosynthesis	Flavones and flavonols (3-hydroxyflavones) are common flavonoids in the plant kingdom. They are synthesized as part of the flavonoid modification pathways in aglycone and glucoside forms.
map00941	Flavonoid biosynthesis	Flavonoids are a major class of plant secondary metabolites that serves a multitude of functions including pigments and antioxidant activity. Flavonoids are synthesized from phenylpropanoid derivatives by condensation with malonyl-CoA. For example, condensation of p-coumaroyl-CoA (C6-C3) with three malonyl-CoA (C3) molecules results in naringenin chalcone with a diphenylpropane (C6-C3-C6) unit, which is converted to naringenin with the flavone (2-phenylchromen-4-one) backbone by conjugate ring closure. These and further modifications yield a variety of structural forms including chalcones, flavanones, dihyroflavonols, and flavans, anthocyanins, flavones and flavonols, and isoflavonoids.