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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_result (5)
Expr_patternExpr1015628
Expr1147743
Expr2011173
Expr2029409
Drives_constructWBCnstr00037058
Construct_productWBCnstr00037058
Microarray_results (19)
Expression_cluster (337)
InteractionWBInteraction000139802
WBInteraction000139803
WBInteraction000139804
WBInteraction000139855
WBInteraction000139915
WBInteraction000140000
WBInteraction000140406
WBInteraction000140408
WBInteraction000140426
WBInteraction000143665
WBInteraction000184422
WBInteraction000187261
WBInteraction000198595
WBInteraction000206421
WBInteraction000206422
WBInteraction000206423
WBInteraction000206424
WBInteraction000206425
WBInteraction000216225
WBInteraction000219555
WBInteraction000278758
WBInteraction000293602
WBInteraction000310801
WBInteraction000339046
WBInteraction000369702
WBInteraction000372768
WBInteraction000394619
WBInteraction000463483
WBInteraction000466263
WBInteraction000466348
WBInteraction000502081
WBInteraction000504532
WBInteraction000504918
WBInteraction000517886
WBInteraction000569007
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