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WormBase Tree Display for Gene: WBGene00010705

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Name Class

WBGene00010705SMapS_parentSequenceK09A11
IdentityVersion2
NameCGC_namecyp-14A1
Sequence_nameK09A11.2
Molecular_nameK09A11.2
K09A11.2.1
CE03473
Other_nameCELE_K09A11.2Accession_evidenceNDBBX284606
Public_namecyp-14A1
DB_infoDatabaseAceViewgeneXN884
WormQTLgeneWBGene00010705
WormFluxgeneWBGene00010705
NDBlocus_tagCELE_K09A11.2
PanthergeneCAEEL|WormBase=WBGene00010705|UniProtKB=Q27506
familyPTHR24284
NCBIgene187183
RefSeqproteinNM_077802.5
TrEMBLUniProtAccQ27506
UniProt_GCRPUniProtAccQ27506
OMIMgene610670
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
221 Sep 2004 09:38:16WBPerson1971Name_changeCGC_namecyp-14A1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcyp
Allele (45)
RNASeq_FPKM (74)
GO_annotation00079911
00079912
00079913
00079914
00118047
00118048
00118049
00118050
Ortholog (55)
Paralog (42)
Structured_descriptionConcise_descriptioncyp-14A1 encodes one of ~80 C. elegans cytochrome P450s: membrane-associated, heme-containing NADPH-dependent monooxygenases that catalyze the oxidative metabolism of a variety of exogenous compounds and endogenous substrates.Curator_confirmedWBPerson1843
Date_last_updated20 Nov 2008 00:00:00
Automated_descriptionPredicted to enable heme binding activity; iron ion binding activity; and oxidoreductase activity. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in several diseases, including autoimmune hepatitis; hematologic cancer (multiple); and hereditary spastic paraplegia 56. Is an ortholog of several human genes including CYP2D6 (cytochrome P450 family 2 subfamily D member 6); CYP2D7 (cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)); and CYP2W1 (cytochrome P450 family 2 subfamily W member 1).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 (12)
Molecular_infoCorresponding_CDSK09A11.2
Corresponding_transcriptK09A11.2.1
Other_sequenceEY468469.1
PPC09763_1
Associated_featureWBsf982263
WBsf238117
Experimental_infoRNAi_resultWBRNAi00050360Inferred_automaticallyRNAi_primary
WBRNAi00034174Inferred_automaticallyRNAi_primary
WBRNAi00092632Inferred_automaticallyRNAi_primary
WBRNAi00116299Inferred_automaticallyRNAi_primary
WBRNAi00016859Inferred_automaticallyRNAi_primary
Expr_patternExpr1015287
Expr1154065
Expr2010691
Expr2028930
Drives_constructWBCnstr00031204
Construct_productWBCnstr00031204
Microarray_results (18)
Expression_cluster (188)
InteractionWBInteraction000155640
WBInteraction000156224
Map_infoMapXPosition11.0455
PositivePositive_cloneK09A11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00063971
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