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WormBase Tree Display for Gene: WBGene00018283

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Name Class

WBGene00018283SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameCGC_namesulp-3Person_evidenceWBPerson2233
Sequence_nameF41D9.5
Molecular_nameF41D9.5
F41D9.5.1
CE38957
Other_nameCELE_F41D9.5Accession_evidenceNDBBX284606
Public_namesulp-3
DB_infoDatabaseAceViewgeneXJ22
WormQTLgeneWBGene00018283
WormFluxgeneWBGene00018283
NDBlocus_tagCELE_F41D9.5
PanthergeneCAEEL|WormBase=WBGene00018283|UniProtKB=Q94225
familyPTHR11814
NCBIgene181094
RefSeqproteinNM_077023.5
SwissProtUniProtAccQ94225
UniProt_GCRPUniProtAccQ94225
OMIMgene604943
608480
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:00WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 Jan 2005 16:30:54WBPerson2970Name_changeCGC_namesulp-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsulp
Allele (91)
StrainWBStrain00036650
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (54)
ParalogWBGene00010788Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010789Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00012259Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013963Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016945Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017464Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020914Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionsulp-3 encodes one of eight C. elegans members of the sulfate permease family of anion transporters; by homology, SULP-3 is predicted to function as an anion transporter that regulates cellular pH and volume via transmembrane movement of electrolytes and fluids; a sulp-3::GFP transcriptional fusion is expressed exclusively in the pharyngeal muscles.Paper_evidenceWBPaper00025075
Curator_confirmedWBPerson1843
Date_last_updated13 Sep 2006 00:00:00
Automated_descriptionPredicted to enable salt transmembrane transporter activity. Predicted to be involved in inorganic anion transmembrane transport and organic anion transport. Predicted to be located in membrane. Expressed in pm3; pm4; pm5; pm6; and pm7. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 61 and spermatogenic failure 3. Is an ortholog of several human genes including SLC26A6 (solute carrier family 26 member 6); SLC26A7 (solute carrier family 26 member 7); and SLC26A9 (solute carrier family 26 member 9).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:0110513Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9359)
DOID:0070168Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14468)
Molecular_infoCorresponding_CDSF41D9.5
Corresponding_CDS_historyF41D9.5:wp146
Corresponding_transcriptF41D9.5.1
Other_sequence (11)
Associated_featureWBsf670837
WBsf982212
WBsf1006134
WBsf1006135
WBsf1006136
WBsf1006137
WBsf1006138
WBsf1023404
WBsf1023405
WBsf237678
Experimental_infoRNAi_resultWBRNAi00032088Inferred_automaticallyRNAi_primary
WBRNAi00000282Inferred_automaticallyRNAi_primary
WBRNAi00046985Inferred_automaticallyRNAi_primary
Expr_patternExpr3248
Expr1026310
Expr1150848
Expr2017114
Expr2035250
Drives_constructWBCnstr00006120
WBCnstr00006121
WBCnstr00009026
WBCnstr00011251
WBCnstr00026638
Construct_productWBCnstr00026638
Microarray_results (18)
Expression_cluster (114)
Interaction (22)
Map_infoMapXPosition-0.128164Error0.005281
PositivePositive_cloneF41D9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00025075
WBPaper00035539
WBPaper00038491
WBPaper00055090
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