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WormBase Tree Display for Gene: WBGene00001154

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Name Class

WBGene00001154EvidencePerson_evidenceWBPerson3205
Author_evidenceVan Gilst M
SMapS_parentSequenceF56B3
IdentityVersion1
NameCGC_nameech-5
Sequence_nameF56B3.5
Molecular_nameF56B3.5
F56B3.5.1
CE46392
Other_nameCELE_F56B3.5Accession_evidenceNDBBX284604
Public_nameech-5
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classech
Allele (56)
StrainWBStrain00001181
RNASeq_FPKM (74)
GO_annotation00033887
00033888
00033889
Contained_in_operonCEOP4040
Ortholog (37)
ParalogWBGene00001155Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016325Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001156Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001151Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001152Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007130Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017301Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019022Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021296Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be involved in fatty acid beta-oxidation. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in 3-methylglutaconic aciduria type 1 and renal tubular transport disease. Is an ortholog of human AUH (AU RNA binding methylglutaconyl-CoA hydratase) and ECHDC2 (enoyl-CoA hydratase domain containing 2).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:0110002Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:890)
DOID:447Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:890)
Molecular_infoCorresponding_CDSF56B3.5
Corresponding_CDS_historyF56B3.5:wp227
Corresponding_transcriptF56B3.5.1
Other_sequence (38)
Associated_featureWBsf645771
WBsf227883
Experimental_infoRNAi_resultWBRNAi00048636Inferred_automaticallyRNAi_primary
Expr_patternChronogram1641
Expr6211
Expr1013162
Expr1030734
Expr1152402
Expr2011169
Expr2029405
Drives_constructWBCnstr00002073
Microarray_results (19)
Expression_cluster (95)
Interaction (44)
Map_infoMapIVPosition-23.422Error0.017026
PositivePositive_cloneF56B3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029292
WBPaper00038491
WBPaper00042257
WBPaper00055090
WBPaper00064080
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