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WormBase Tree Display for Gene: WBGene00017012

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Name Class

WBGene00017012SMapS_parentSequenceD1009
IdentityVersion2
NameCGC_nameacs-22Person_evidenceWBPerson237
WBPerson9275
Sequence_nameD1009.1
Molecular_nameD1009.1a
D1009.1a.1
CE04285
D1009.1c
CE51329
D1009.1d
CE51246
D1009.1c.1
D1009.1d.1
Other_nameCELE_D1009.1Accession_evidenceNDBBX284606
Public_nameacs-22
DB_infoDatabaseAceViewgeneXJ557
WormQTLgeneWBGene00017012
WormFluxgeneWBGene00017012
NDBlocus_tagCELE_D1009.1
PanthergeneCAEEL|WormBase=WBGene00017012|UniProtKB=Q18916
familyPTHR43107
NCBIgene181138
RefSeqproteinNM_001392815.1
NM_001322629.4
NM_077108.6
TrEMBLUniProtAccQ18916
A0A131MBB2
A0A131MB92
UniProt_GCRPUniProtAccQ18916
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
213 Mar 2009 14:10:25WBPerson9133Name_changeCGC_nameacs-22
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacs
Allele (144)
StrainWBStrain00004763
RNASeq_FPKM (74)
GO_annotation00001951
00001952
00001953
00001954
00001955
00001956
00001957
00062816
Ortholog (44)
Paralog (17)
Structured_descriptionConcise_descriptionacs-22 encodes a protein homologous to the mammalian FATP1 and FATP4 fatty acid transport proteins (FATP)/very long chain fatty acid acyl-CoA synthetases; acs-22 functions redundantly with acs-20 to regulate formation of the cuticle surface barrier that prevents penetration of small molecules; acs-22 may affect cuticle development via its role in incorporation of very long chain fatty acids, but not other fatty acids, into sphingomyelin; an acs-22::gfp promoter fusion is expressed strongly in the intestine, with weaker expression seen in the pharynx, head neurons, and hypodermis.Paper_evidenceWBPaper00035868
Curator_confirmedWBPerson1843
Date_last_updated03 Feb 2010 00:00:00
Automated_descriptionPredicted to enable long-chain fatty acid transporter activity and long-chain fatty acid-CoA ligase activity. Predicted to be involved in triglyceride homeostasis. Located in endoplasmic reticulum. Expressed in head neurons; hypodermis; and pharynx. Human ortholog(s) of this gene implicated in obesity. Is an ortholog of human SLC27A1 (solute carrier family 27 member 1) and SLC27A4 (solute carrier family 27 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:9970Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10998)
Molecular_infoCorresponding_CDSD1009.1a
D1009.1c
D1009.1d
Corresponding_CDS_historyD1009.1b:wp271
Corresponding_transcriptD1009.1a.1
D1009.1c.1
D1009.1d.1
Other_sequence (52)
Associated_feature (16)
Experimental_infoRNAi_resultWBRNAi00043335Inferred_automaticallyRNAi_primary
WBRNAi00012490Inferred_automaticallyRNAi_primary
WBRNAi00030314Inferred_automaticallyRNAi_primary
WBRNAi00092595Inferred_automaticallyRNAi_primary
Expr_patternExpr8894
Expr1020922
Expr1037310
Expr1147315
Expr2009212
Expr2027449
Drives_constructWBCnstr00013588
WBCnstr00022751
WBCnstr00027639
Construct_productWBCnstr00014925
WBCnstr00022756
WBCnstr00027639
Microarray_results (28)
Expression_cluster (202)
Interaction (87)
Map_infoMapXPosition0.449566Error0.000197
PositivePositive_cloneD1009Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (15)
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