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WormBase Tree Display for Gene: WBGene00015400

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Name Class

WBGene00015400SMapS_parentSequenceC03G6
IdentityVersion2
NameCGC_namecyp-35A2
Sequence_nameC03G6.15
Molecular_nameC03G6.15
C03G6.15.1
CE35217
Other_nameCELE_C03G6.15Accession_evidenceNDBBX284605
Public_namecyp-35A2
DB_infoDatabaseAceViewgene5H840
WormQTLgeneWBGene00015400
WormFluxgeneWBGene00015400
NDBlocus_tagCELE_C03G6.15
PanthergeneCAEEL|WormBase=WBGene00015400|UniProtKB=O02628
familyPTHR24300
NCBIgene182177
RefSeqproteinNM_072479.7
TrEMBLUniProtAccO02628
UniProt_GCRPUniProtAccO02628
OMIMgene601130
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
221 Sep 2004 09:38:16WBPerson1971Name_changeCGC_namecyp-35A2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcyp
Allele (33)
StrainWBStrain00036000
WBStrain00036030
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (177)
Paralog (44)
Structured_descriptionConcise_descriptioncyp-35A2 encodes one of over 80 C. elegans cytochrome P450s, NADPH-dependent monooxygenases that metabolize endogenous and exogenous compounds; RT-PCR experiments indicate that cyp-35A2 mRNA is upregulated in response to treatment with xenobiotics, such as PCBs (polychlorinated biphenyls) or PAHs (polycyclic aromatic hydrocarbons); loss of cyp-35A/C gene family activity in the presence of xenobiotics can diminish the reproductive decline seen in wild-type worms treated with the same compounds; in addition, cyp-35A(RNAi) also results in a reduction of fat content; cyp-35A2 reporter gene fusions are strongly expressed in the intestine following treatment with xenobiotics.Paper_evidenceWBPaper00004966
WBPaper00005655
WBPaper00025207
WBPaper00031939
Curator_confirmedWBPerson1843
Date_last_updated26 Feb 2009 00:00:00
Automated_descriptionPredicted to enable heme binding activity; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen; and steroid hydroxylase activity. Involved in response to xenobiotic stimulus. Predicted to be located in cytoplasm and intracellular membrane-bounded organelle. Expressed in intestine. Human ortholog(s) of this gene implicated in several diseases, including gastrointestinal system cancer (multiple); glucose metabolism disease (multiple); and lung disease (multiple). Is an ortholog of several human genes including CYP2A13 (cytochrome P450 family 2 subfamily A member 13); CYP2A6 (cytochrome P450 family 2 subfamily A member 6); and CYP2A7 (cytochrome P450 family 2 subfamily A member 7).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_model (57)
Molecular_infoCorresponding_CDSC03G6.15
Corresponding_CDS_historyC03G6.15:wp106
Corresponding_transcriptC03G6.15.1
Other_sequenceES740345.1
Tcol_isotig20275
Associated_featureWBsf652771
WBsf669117
WBsf233940
Experimental_infoRNAi_resultWBRNAi00039543Inferred_automaticallyRNAi_primary
WBRNAi00116295Inferred_automaticallyRNAi_primary
WBRNAi00092682Inferred_automaticallyRNAi_primary
WBRNAi00010068Inferred_automaticallyRNAi_primary
WBRNAi00114818Inferred_automaticallyRNAi_primary
WBRNAi00078475Inferred_automaticallyRNAi_primary
WBRNAi00106221Inferred_automaticallyRNAi_primary
WBRNAi00028398Inferred_automaticallyRNAi_primary
Expr_patternExpr1683
Expr8189
Expr11595
Expr1029051
Expr1036590
Expr1143647
Expr2010735
Expr2028972
Drives_constructWBCnstr00004995
WBCnstr00010373
WBCnstr00019076
WBCnstr00028873
Construct_productWBCnstr00019076
WBCnstr00028873
Microarray_results (14)
Expression_cluster (292)
Interaction (49)
Map_infoMapVPosition0.715015Error0.002421
PositivePositive_cloneC03G6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5576
Pseudo_map_position
Reference (27)
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene