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WormBase Tree Display for Gene: WBGene00019565

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Name Class

WBGene00019565SMapS_parentSequenceK09D9
IdentityVersion2
NameCGC_namecyp-35A3
Sequence_nameK09D9.2
Molecular_nameK09D9.2
K09D9.2.1
CE21056
Other_nameCELE_K09D9.2Accession_evidenceNDBBX284605
Public_namecyp-35A3
DB_infoDatabaseAceViewgene5E497
WormQTLgeneWBGene00019565
WormFluxgeneWBGene00019565
NDBlocus_tagCELE_K09D9.2
PanthergeneCAEEL|WormBase=WBGene00019565|UniProtKB=Q9N5I1
familyPTHR24300
NCBIgene187209
RefSeqproteinNM_071720.6
TrEMBLUniProtAccQ9N5I1
UniProt_GCRPUniProtAccQ9N5I1
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
221 Sep 2004 09:38:16WBPerson1971Name_changeCGC_namecyp-35A3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcyp
Allele (50)
StrainWBStrain00032730
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (172)
Paralog (44)
Structured_descriptionConcise_descriptioncyp-35A3 encodes one of over 80 C. elegans cytochrome P450s, NADPH-dependent monooxygenases that metabolize endogenous and exogenous compounds; 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-35A3 reporter gene fusions are strongly expressed in the intestine following treatment with xenobiotics.Paper_evidenceWBPaper00005655
WBPaper00025207
WBPaper00029387
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. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); gastrointestinal system cancer (multiple); and lung disease (multiple). Is an ortholog of several human genes including CYP2B6 (cytochrome P450 family 2 subfamily B member 6); CYP2D6 (cytochrome P450 family 2 subfamily D member 6); and CYP2D7 (cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)).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 (42)
Molecular_infoCorresponding_CDSK09D9.2
Corresponding_transcriptK09D9.2.1
Other_sequenceEY459839.1
Associated_featureWBsf646734
WBsf978993
WBsf231624
Experimental_infoRNAi_result (15)
Expr_patternExpr4664
Expr1038451
Expr1154117
Expr2010736
Expr2028973
Drives_constructWBCnstr00012158
WBCnstr00025764
Construct_productWBCnstr00025764
Microarray_results (15)
Expression_cluster (296)
Interaction (28)
Map_infoMapVPosition-7.01998Error0.006429
PositivePositive_cloneK09D9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (16)
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