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WormBase Tree Display for Gene: WBGene00007129

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Name Class

WBGene00007129SMapS_parentSequenceB0272
IdentityVersion1
NameSequence_nameB0272.3
Molecular_nameB0272.3
B0272.3.1
CE00852
Other_nameCELE_B0272.3Accession_evidenceNDBBX284606
Public_nameB0272.3
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:47WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (25)
StrainWBStrain00003159
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (33)
ParalogWBGene00010035Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00019978Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001150Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001157Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001158Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020347Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022130Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionB0272.3 encodes a 3-hydroxyacyl-CoA dehydrogenase; by homology, the product of B0272.3 is predicted to function in mitochondrial fatty acid metabolism by catalyzing the NAD+-dependent oxidation of short-chain hydroxyacyl CoAs; large-scale expression studies indicate that B0272.3 is widely expressed.Paper_evidenceWBPaper00031006
Curator_confirmedWBPerson1843
Date_last_updated11 Nov 2008 00:00:00
Automated_descriptionPredicted to enable 3-hydroxyacyl-CoA dehydrogenase activity. Predicted to be involved in fatty acid beta-oxidation. Predicted to be located in mitochondrion. Expressed widely. Human ortholog(s) of this gene implicated in familial hyperinsulinemic hypoglycemia 4. Is an ortholog of human HADH (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:0070215Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4799)
Molecular_infoCorresponding_CDSB0272.3
Corresponding_transcriptB0272.3.1
Other_sequence (102)
Associated_featureWBsf648410
WBsf1006429
WBsf1023558
WBsf236161
Experimental_infoRNAi_resultWBRNAi00102622Inferred_automaticallyRNAi_primary
WBRNAi00038826Inferred_automaticallyRNAi_primary
WBRNAi00009645Inferred_automaticallyRNAi_primary
WBRNAi00028042Inferred_automaticallyRNAi_primary
WBRNAi00090695Inferred_automaticallyRNAi_primary
Expr_patternChronogram2006
Expr70
Expr5032
Expr1012851
Expr1033066
Expr1143029
Expr2000105
Expr2018321
Drives_constructWBCnstr00003637
WBCnstr00033976
Construct_productWBCnstr00033976
Microarray_results (19)
Expression_cluster (140)
Interaction (13)
Map_infoPositivePositive_cloneB0272Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX1.20398
ReferenceWBPaper00026800
WBPaper00038491
WBPaper00042257
WBPaper00049828
WBPaper00055090
MethodGene