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WormBase Tree Display for Gene: WBGene00008598

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Name Class

WBGene00008598SMapS_parentSequenceF09A5
IdentityVersion2
NameCGC_namespin-3Paper_evidenceWBPaper00042308
Sequence_nameF09A5.1
Molecular_nameF09A5.1
F09A5.1.1
CE40809
Other_nameCELE_F09A5.1Accession_evidenceNDBBX284606
Public_namespin-3
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
204 Jun 2013 14:47:04WBPerson2970Name_changeCGC_namespin-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classspin
Allele (64)
StrainWBStrain00032469
RNASeq_FPKM (74)
GO_annotation00063987
00063988
00063989
00116490
00116491
Ortholog (55)
ParalogWBGene00007549Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00008033Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013739Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Expressed in amphid neurons; intestine; and retrovesicular ganglion neurons. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 115. Is an ortholog of human SPNS1 (SPNS lysolipid transporter 1, lysophospholipid); SPNS2 (SPNS lysolipid transporter 2, sphingosine-1-phosphate); and SPNS3 (SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)).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:0111643Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:26992)
Molecular_infoCorresponding_CDSF09A5.1
Corresponding_CDS_historyF09A5.1:wp102
F09A5.1:wp173
Corresponding_transcriptF09A5.1.1
Other_sequenceHC05598
ACC16946_1
EY471708.1
Dviv_isotig17614
HCC07391_1
Dviv_isotig17615
Associated_featureWBsf236537
Experimental_infoRNAi_resultWBRNAi00030682Inferred_automaticallyRNAi_primary
WBRNAi00044069Inferred_automaticallyRNAi_primary
WBRNAi00012942Inferred_automaticallyRNAi_primary
Expr_patternExpr13201
Expr1026100
Expr1148034
Expr2034294
Drives_constructWBCnstr00032841
WBCnstr00038866
Construct_productWBCnstr00032841
Microarray_results (18)
Expression_cluster (154)
Interaction (11)
Map_infoMapXPosition10.2128
PositivePositive_cloneF09A5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00061938
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