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WormBase Tree Display for Gene: WBGene00018152

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Name Class

WBGene00018152SMapS_parentSequenceF37C12
IdentityVersion2
NameCGC_nameacs-4Paper_evidenceWBPaper00031915
Person_evidenceWBPerson2239
WBPerson237
WBPerson7030
Sequence_nameF37C12.7
Molecular_nameF37C12.7
F37C12.7.1
CE29312
Other_nameCELE_F37C12.7Accession_evidenceNDBBX284603
Public_nameacs-4
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
217 Apr 2008 14:07:55WBPerson2970Name_changeCGC_nameacs-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacs
Allele (51)
StrainWBStrain00037194
Component_of_genotypeWBGenotype00000108
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (50)
Paralog (17)
Structured_descriptionAutomated_descriptionPredicted to enable long-chain fatty acid-CoA ligase activity. Predicted to be involved in long-chain fatty acid metabolic process; long-chain fatty-acyl-CoA metabolic process; and neuron differentiation. Located in lipid droplet. Expressed in hypodermis; intestine; pharynx; and somatic nervous system. Human ortholog(s) of this gene implicated in several diseases, including lung cancer; non-syndromic X-linked intellectual disability 63; and prostate cancer. Is an ortholog of human ACSL3 (acyl-CoA synthetase long chain family member 3) and ACSL4 (acyl-CoA synthetase long chain family member 4).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:10283Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3570)
DOID:1324Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3570)
DOID:0112050Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3571)
DOID:2841Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3570)
DOID:1059Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3571)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3570)
Molecular_infoCorresponding_CDSF37C12.7
Corresponding_transcriptF37C12.7.1
Other_sequence (70)
Associated_featureWBsf654974
WBsf992953
WBsf1015200
WBsf225201
WBsf225202
WBsf225203
WBsf225204
WBsf225205
Experimental_infoRNAi_result (21)
Expr_patternExpr8137
Expr12153
Expr12398
Expr1011255
Expr1037819
Expr1150500
Expr2009215
Expr2027452
Drives_constructWBCnstr00013136
WBCnstr00020292
WBCnstr00026742
Construct_productWBCnstr00026742
WBCnstr00038689
Microarray_results (21)
Expression_cluster (163)
Interaction (106)
Map_infoMapIIIPosition-0.777808Error0.000168
PositivePositive_cloneF37C12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
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