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WormBase Tree Display for Gene: WBGene00009218

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Name Class

WBGene00009218SMapS_parentSequenceF28D1
IdentityVersion2
NameCGC_nameacs-20Person_evidenceWBPerson237
WBPerson2239
Sequence_nameF28D1.9
Molecular_nameF28D1.9
F28D1.9.1
CE47963
Other_nameCELE_F28D1.9Accession_evidenceNDBBX284604
Public_nameacs-20
DB_infoDatabaseAceViewgene4N158
WormQTLgeneWBGene00009218
WormFluxgeneWBGene00009218
NDBlocus_tagCELE_F28D1.9
PanthergeneCAEEL|WormBase=WBGene00009218|UniProtKB=Q19878
familyPTHR43107
NCBIgene178190
RefSeqproteinNM_069966.10
TrEMBLUniProtAccQ19878
UniProt_GCRPUniProtAccQ19878
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
211 Sep 2008 09:57:25WBPerson2970Name_changeCGC_nameacs-20
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacs
AlleleWBVar02148836Inferred_automaticallyFrom strain object: CB7109
From strain object: CB7198
WBVar01398353
WBVar01500079
WBVar02134825
WBVar01859356
WBVar01859357
WBVar01859358
WBVar01859359
WBVar01859360
WBVar01859361
WBVar01498811
WBVar01498996
WBVar00260790
WBVar01499925
WBVar00948303
WBVar00948304
WBVar00948305
WBVar00948306
WBVar00948307
WBVar01569800
WBVar00948308
WBVar01569801
WBVar00948309
WBVar01569802
WBVar00948310
WBVar01569803
WBVar00948311
WBVar01569804
WBVar01569805
WBVar00948312
WBVar01569806
WBVar00948313
WBVar02037281
WBVar00948314
WBVar00437729
WBVar00437730
WBVar01731312
WBVar02037282
WBVar00948315
WBVar01482458
WBVar00437731
WBVar00948316
WBVar00437732
WBVar00948317
WBVar00437733
WBVar02059367
WBVar00948318
WBVar00948319
WBVar02059368
WBVar00437734
WBVar00437735
WBVar00948320
WBVar00948321
WBVar00437736
WBVar00948322
WBVar00437737
WBVar00948323
WBVar00437738
WBVar00437739
WBVar00948324
WBVar00437740
WBVar00948325
WBVar00437741
WBVar00948326
WBVar00948327
WBVar00948328
WBVar00948329
WBVar02088279
WBVar00251979
WBVar00574613
WBVar00574615
WBVar01498688
WBVar00252008
WBVar01967185
WBVar01496861
WBVar01954027
WBVar01954028
WBVar00276443
WBVar01454563
WBVar01454564
WBVar01454565
WBVar01454566
WBVar01454567
WBVar00602811
WBVar00255764
WBVar01500245
WBVar02021344
WBVar01498775
Strain (2)
RNASeq_FPKM (74)
GO_annotation00066220
00066221
00066222
00066223
00066224
00066225
00066226
00066227
Ortholog (42)
Paralog (17)
Structured_descriptionConcise_descriptionacs-20 encodes a protein homologous to the mammalian FATP1 and FATP4 fatty acid transport proteins (FATP)/very long chain fatty acid acyl-CoA synthetases; acs-20 activity is required for proper cuticle development, specifically formation of a cuticle surface barrier that prevents penetration of small molecules; acs-20 may affect cuticle development via its role in incorporation of very long chain fatty acids, but not other fatty acids, into sphingomyelin; acs-20; acs-22 doubly mutant animals have moresevere cuticle barrier defects than acs-20 single mutants, suggesting that the two genes function redundantly; acs-20 defects can be rescued by human Fatp4; an ACS-20::GFP fusion protein is expressed in the hyp7 and seam hypodermis, as well as the vulval and anal muscles; in hypodermal cells, ACS-20 localizes in a reticular pattern suggestive of localization to the endoplasmic reticulum.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 intracellular membrane-bounded organelle. Expressed in anal depressor muscle; anal sphincter muscle; head; hyp7 syncytium; and seam cell. 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_CDSF28D1.9
Corresponding_CDS_historyF28D1.9:wp154
Corresponding_transcriptF28D1.9.1
Other_sequence (33)
Associated_feature (13)
Experimental_infoRNAi_result (23)
Expr_patternChronogram984
Expr5903
Expr8893
Expr8895
Expr1026843
Expr1034021
Expr1149741
Expr2009210
Expr2027447
Drives_constructWBCnstr00002507
WBCnstr00007265
WBCnstr00013587
WBCnstr00013589
WBCnstr00022750
WBCnstr00022752
WBCnstr00032361
Construct_productWBCnstr00007265
WBCnstr00013589
WBCnstr00022752
WBCnstr00022754
WBCnstr00032361
Microarray_results (17)
Expression_cluster (233)
Interaction (173)
Map_infoMapIVPosition5.90843Error0.002883
PositivePositive_cloneF28D1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
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