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WormBase Tree Display for Gene: WBGene00001158

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Name Class

WBGene00001158EvidencePerson_evidenceWBPerson3205
Author_evidenceVan Gilst M
SMapS_parentSequenceF01G10
IdentityVersion1
NameCGC_nameech-9
Sequence_nameF01G10.3
Molecular_nameF01G10.3a
F01G10.3a.1
CE35451
F01G10.3b
CE49962
F01G10.3b.1
Other_nameCELE_F01G10.3Accession_evidenceNDBBX284604
Public_nameech-9
DB_infoDatabaseAceViewgene4K998
WormQTLgeneWBGene00001158
WormFluxgeneWBGene00001158
NDBlocus_tagCELE_F01G10.3
PanthergeneCAEEL|WormBase=WBGene00001158|UniProtKB=O17762
familyPTHR23309
NCBIgene184065
RefSeqproteinNM_069474.6
NM_001380437.1
TrEMBLUniProtAccA0A061AKU6
O17762
UniProt_GCRPUniProtAccO17762
OMIMgene607037
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classech
Allele (45)
RNASeq_FPKM (74)
GO_annotation00000391
00000392
00000393
00030660
00108339
00108340
00108341
00108342
Ortholog (29)
ParalogWBGene00001157Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00001150Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007129Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00010035Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019978Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020347Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022130Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable 3-hydroxyacyl-CoA dehydrogenase activity. Predicted to be involved in fatty acid beta-oxidation. Predicted to be located in peroxisome. Human ortholog(s) of this gene implicated in Fanconi renotubular syndrome 3. Is an ortholog of human EHHADH (enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase).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:0080759Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3247)
Molecular_infoCorresponding_CDSF01G10.3a
F01G10.3b
Corresponding_CDS_historyF01G10.3:wp109
Corresponding_transcriptF01G10.3a.1
F01G10.3b.1
Other_sequenceCRC08797_1
FG980875.1
HBC12703_1
Tcol_isotig17282
CR12067
Tcir_isotig23141
Tcol_isotig21554
Associated_featureWBsf230703
Experimental_infoRNAi_resultWBRNAi00030549Inferred_automaticallyRNAi_primary
WBRNAi00082449Inferred_automaticallyRNAi_primary
WBRNAi00102620Inferred_automaticallyRNAi_primary
WBRNAi00012745Inferred_automaticallyRNAi_primary
WBRNAi00043765Inferred_automaticallyRNAi_primary
Expr_patternExpr1015628
Expr1147743
Expr2011173
Expr2029409
Drives_constructWBCnstr00037058
Construct_productWBCnstr00037058
Microarray_results (19)
Expression_cluster (337)
Interaction (35)
Map_infoMapIVPosition4.56237
PositivePositive_cloneF01G10Inferred_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