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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_construct (3)
Construct_productWBCnstr00014925
WBCnstr00022756
WBCnstr00027639
Microarray_results (28)
Expression_cluster (202)
InteractionWBInteraction000046042
WBInteraction000046044
WBInteraction000046046
WBInteraction000046048
WBInteraction000046050
WBInteraction000104129
WBInteraction000110934
WBInteraction000120834
WBInteraction000120835
WBInteraction000122030
WBInteraction000134978
WBInteraction000135291
WBInteraction000140229
WBInteraction000140639
WBInteraction000142808
WBInteraction000148768
WBInteraction000150656
WBInteraction000150657
WBInteraction000163655
WBInteraction000174786
WBInteraction000178033
WBInteraction000180825
WBInteraction000185141
WBInteraction000185148
WBInteraction000185160
WBInteraction000186024
WBInteraction000186046
WBInteraction000195117
WBInteraction000203750
WBInteraction000204859
WBInteraction000211735
WBInteraction000217036
WBInteraction000226727
WBInteraction000229114
WBInteraction000229805
WBInteraction000234217
WBInteraction000236446
WBInteraction000236447
WBInteraction000237334
WBInteraction000242799
WBInteraction000244300
WBInteraction000245349
WBInteraction000253729
WBInteraction000261152
WBInteraction000262769
WBInteraction000273577
WBInteraction000273578
WBInteraction000277171
WBInteraction000282597
WBInteraction000284928
WBInteraction000285472
WBInteraction000311776
WBInteraction000314240
WBInteraction000331300
WBInteraction000333128
WBInteraction000346976
WBInteraction000349431
WBInteraction000364545
WBInteraction000364658
WBInteraction000367404
WBInteraction000367801
WBInteraction000374101
WBInteraction000401645
WBInteraction000406577
WBInteraction000408515
WBInteraction000418659
WBInteraction000437997
WBInteraction000443120
WBInteraction000444007
WBInteraction000444105
WBInteraction000461560
WBInteraction000462276
WBInteraction000462588
WBInteraction000462810
WBInteraction000463578
WBInteraction000464508
WBInteraction000465834
WBInteraction000469140
WBInteraction000540419
WBInteraction000541908
WBInteraction000563034
WBInteraction000563617
WBInteraction000575312
WBInteraction000579752
WBInteraction000583409
WBInteraction000585807
WBInteraction000586567
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