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WormBase Tree Display for Gene: WBGene00013739

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Name Class

WBGene00013739SMapS_parentSequenceY111B2A
IdentityVersion2
NameCGC_namespin-4Paper_evidenceWBPaper00042308
Sequence_nameY111B2A.19
Molecular_nameY111B2A.19a
Y111B2A.19a.1
CE52802
Y111B2A.19b
CE52767
Y111B2A.19b.1
Other_nameY111B2G.jCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_Y111B2A.19Accession_evidenceNDBBX284603
Public_namespin-4
DB_infoDatabaseAceViewgene3N783
WormQTLgeneWBGene00013739
WormFluxgeneWBGene00013739
NDBlocus_tagCELE_Y111B2A.19
PanthergeneCAEEL|WormBase=WBGene00013739|UniProtKB=A0A3B1DV80
familyPTHR23505
NCBIgene190952
RefSeqproteinNM_001392221.1
NM_001379966.1
TrEMBLUniProtAccA0A3B1DV80
A0A3B1DQ22
UniProt_GCRPUniProtAccA0A3B1DV80
OMIMgene612584
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:55WBPerson1971EventImportedInitial conversion from CDS class of WS125
204 Jun 2013 14:47:04WBPerson2970Name_changeCGC_namespin-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classspin
Allele (246)
Possibly_affected_byWBVar02158935
StrainWBStrain00032670
RNASeq_FPKM (74)
GO_annotation00003230
00003231
00003232
00120536
00120537
Contained_in_operonCEOP3889
Ortholog (47)
ParalogWBGene00007549Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00008033Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00008598Caenorhabditis 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. 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_CDSY111B2A.19a
Y111B2A.19b
Corresponding_CDS_historyY111B2A.19:wp104
Y111B2A.19:wp267
Corresponding_transcriptY111B2A.19a.1
Y111B2A.19b.1
Other_sequence (27)
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00019884Inferred_automaticallyRNAi_primary
WBRNAi00055352Inferred_automaticallyRNAi_primary
WBRNAi00036573Inferred_automaticallyRNAi_primary
Expr_patternExpr1024267
Expr1036157
Expr1158881
Expr2016059
Expr2034295
Microarray_results (17)
Expression_cluster (87)
InteractionWBInteraction000033877
WBInteraction000168245
WBInteraction000198935
WBInteraction000211519
WBInteraction000295208
Map_infoMapIIIPosition18.198
PositivePositive_cloneY111B2AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00064639
WBPaper00065123
WBPaper00066330
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