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WormBase Tree Display for Gene: WBGene00007549

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Name Class

WBGene00007549SMapS_parentSequenceC13C4
IdentityVersion2
NameCGC_namespin-1Paper_evidenceWBPaper00042308
Sequence_nameC13C4.5
Molecular_nameC13C4.5
C13C4.5.1
CE08130
Other_nameCELE_C13C4.5Accession_evidenceNDBBX284605
Public_namespin-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
204 Jun 2013 14:47:04WBPerson2970Name_changeCGC_namespin-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classspin
Allele (23)
StrainWBStrain00002087
WBStrain00032371
RNASeq_FPKM (74)
GO_annotation00026210
00026211
00026212
00115658
00115659
Ortholog (45)
ParalogWBGene00008033Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00013739Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00008598Caenorhabditis elegansFrom_analysisPanther
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 tail. 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_CDSC13C4.5
Corresponding_transcriptC13C4.5.1
Other_sequence (39)
Associated_featureWBsf661858
WBsf717265
WBsf232605
WBsf232606
Experimental_infoRNAi_resultWBRNAi00090667Inferred_automaticallyRNAi_primary
WBRNAi00066581Inferred_automaticallyRNAi_primary
WBRNAi00010683Inferred_automaticallyRNAi_primary
WBRNAi00040434Inferred_automaticallyRNAi_primary
WBRNAi00102256Inferred_automaticallyRNAi_primary
WBRNAi00028842Inferred_automaticallyRNAi_primary
Expr_patternChronogram1109
Chronogram1192
Expr5253
Expr5254
Expr1011912
Expr1033247
Expr1144499
Expr2016057
Expr2034292
Drives_constructWBCnstr00002249
WBCnstr00004270
WBCnstr00033655
Construct_productWBCnstr00033655
Microarray_results (19)
Expression_cluster (149)
InteractionWBInteraction000028558
WBInteraction000033672
WBInteraction000277018
WBInteraction000373452
WBInteraction000408472
WBInteraction000408606
WBInteraction000543492
WBInteraction000580543
Map_infoMapVPosition3.6627
PositivePositive_cloneC13C4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00042308
WBPaper00055090
WBPaper00062728
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