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WormBase Tree Display for Gene: WBGene00009818

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Name Class

WBGene00009818SMapS_parentSequenceF47B10
IdentityVersion2
NameCGC_nameacbp-3Person_evidenceWBPerson344
Sequence_nameF47B10.7
Molecular_nameF47B10.7
F47B10.7.1
CE32423
Other_nameCELE_F47B10.7Accession_evidenceNDBBX284606
Public_nameacbp-3
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
201 Apr 2005 11:05:24WBPerson2970Name_changeCGC_nameacbp-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacbp
Allele (42)
StrainWBStrain00032450
RNASeq_FPKM (74)
GO_annotation00068338
00068339
00068340
00068341
00068342
00117411
Ortholog (47)
ParalogWBGene00001153Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007680Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016655Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018949Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00044603Caenorhabditis elegansFrom_analysisPanther
WBGene00012457Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionConcise_descriptionacbp-3 encodes a highly conserved protein containing a functional acyl-CoA-binding binding domain required for protein stability and ligand binding; mutant contains approximately 30% fewer lipid droplets and 20% less triglycerides; loss of ACBP-3 results in 35-40% reduction in lipid chain unsaturation; ACBP-3::GFP is predominantly expressed in hypodermis, body wall muscles and pharynx.Paper_evidenceWBPaper00038378
Curator_confirmedWBPerson12884
WBPerson1843
Date_last_updated13 May 2011 00:00:00
Automated_descriptionPredicted to enable fatty-acyl-CoA binding activity. Involved in lipid storage. Predicted to be located in cytoplasm. Expressed in body wall musculature and pharynx. Human ortholog(s) of this gene implicated in retinal dystrophy with leukodystrophy. Is an ortholog of human ACBD4 (acyl-CoA binding domain containing 4) and ACBD5 (acyl-CoA binding domain containing 5).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:0080946Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:23338)
Molecular_infoCorresponding_CDSF47B10.7
Corresponding_CDS_historyF47B10.7:wp90
Corresponding_transcriptF47B10.7.1
Other_sequence (40)
Associated_featureWBsf648503
WBsf663282
WBsf663283
WBsf663284
WBsf718697
WBsf1006846
WBsf236316
Experimental_infoRNAi_resultWBRNAi00015151Inferred_automaticallyRNAi_primary
WBRNAi00047600Inferred_automaticallyRNAi_primary
WBRNAi00032406Inferred_automaticallyRNAi_primary
Expr_patternExpr13618
Expr13621
Expr1026772
Expr1034289
Expr1151436
Expr2009115
Expr2027352
Drives_constructWBCnstr00031895
WBCnstr00039884
Construct_productWBCnstr00031895
WBCnstr00039884
Microarray_results (19)
Expression_cluster (218)
Interaction (55)
Map_infoMapXPosition2.68331Error0.005475
PositivePositive_cloneF47B10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00039062
WBPaper00055090
WBPaper00065315
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