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WormBase Tree Display for Gene: WBGene00012907

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Name Class

WBGene00012907SMapS_parentSequenceY46G5A
IdentityVersion2
NameCGC_namecpt-1Person_evidenceWBPerson3206
WBPerson3205
Sequence_nameY46G5A.17
Molecular_nameY46G5A.17
Y46G5A.17.1
CE36414
Y46G5A.17.2
Other_nameCELE_Y46G5A.17Accession_evidenceNDBBX284602
Public_namecpt-1
DB_infoDatabaseAceViewgene2N80
WormQTLgeneWBGene00012907
WormFluxgeneWBGene00012907
NDBlocus_tagCELE_Y46G5A.17
PanthergeneCAEEL|WormBase=WBGene00012907|UniProtKB=Q9U2F2
familyPTHR22589
NCBIgene174912
RefSeqproteinNM_064320.6
TrEMBLUniProtAccQ9U2F2
UniProt_GCRPUniProtAccQ9U2F2
OMIMgene600528
608846
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
218 Jul 2005 13:34:00WBPerson2970Name_changeCGC_namecpt-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcpt
Allele (342)
StrainWBStrain00001343
RNASeq_FPKM (74)
GO_annotation (16)
Contained_in_operonCEOP2721
Ortholog (60)
ParalogWBGene00000481Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007175Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00008629Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009622Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00011122Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00011850Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021002Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020911Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021703Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00019644Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionY46G5A.17 is orthologous to the human gene SIMILAR TO CARNITINE PALMITOYLTRANSFERASE I, LIVER (CPT1A; OMIM:600528), which when mutated leads to disease.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated06 Aug 2004 00:00:00
Automated_descriptionPredicted to enable carnitine O-palmitoyltransferase activity. Predicted to be involved in carnitine metabolic process and fatty acid metabolic process. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in carnitine palmitoyltransferase I deficiency; hereditary spastic paraplegia 73; and lymphangioleiomyomatosis. Is an ortholog of human CPT1A (carnitine palmitoyltransferase 1A) and CPT1C (carnitine palmitoyltransferase 1C).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_modelDOID:0110818Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18540)
DOID:0090129Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2328)
DOID:3319Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2328)
DOID:3146Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2328)
Molecular_infoCorresponding_CDSY46G5A.17
Corresponding_CDS_historyY46G5A.17:wp52
Y46G5A.17:wp119
Corresponding_transcriptY46G5A.17.1
Y46G5A.17.2
Other_sequence (115)
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00056674Inferred_automaticallyRNAi_primary
WBRNAi00000348Inferred_automaticallyRNAi_primary
Expr_patternChronogram1623
Expr6984
Expr1011554
Expr1035713
Expr1160145
Expr2010514
Expr2028754
Drives_constructWBCnstr00002236
WBCnstr00029794
Construct_productWBCnstr00029794
Microarray_results (19)
Expression_cluster (151)
InteractionWBInteraction000558548
WBInteraction000563740
WBInteraction000579824
WBInteraction000585689
Map_infoMapIIPosition11.205Error0.026807
PositivePositive_cloneY46G5AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
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