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WormBase Tree Display for Gene: WBGene00012259

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Name Class

WBGene00012259SMapS_parentSequenceW04G3
IdentityVersion3
NameCGC_namesulp-7Person_evidenceWBPerson2233
Sequence_nameW04G3.6
Molecular_name (12)
Other_nameCELE_W04G3.6Accession_evidenceNDBBX284606
Public_namesulp-7
DB_infoDatabaseWormQTLgeneWBGene00012259
WormFluxgeneWBGene00012259
NDBlocus_tagCELE_W04G3.6
PanthergeneCAEEL|WormBase=WBGene00012259|UniProtKB=G5EC30
familyPTHR11814
NCBIgene189195
RefSeqproteinNM_001038479.2
NM_001038482.4
NM_001038481.4
NM_001038480.2
TrEMBLUniProtAccG5EFX9
G5EGG6
G5EC30
G5EE27
UniProt_GCRPUniProtAccG5EC30
OMIMgene126650
604943
605646
606718
610130
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:53WBPerson1971EventImportedInitial conversion from CDS class of WS125
220 Oct 2004 18:04:32WBPerson1846EventAcquires_mergeWBGene00012262
319 Jan 2005 16:30:54WBPerson2970Name_changeCGC_namesulp-7
Acquires_mergeWBGene00012262
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsulp
Allele (93)
StrainWBStrain00037626
WBStrain00037645
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (48)
ParalogWBGene00010788Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010789Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013963Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00018283Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020914Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016945Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017464Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionsulp-7 encodes one of eight C. elegans members of the sulfate permease family of anion transporters; by homology, SULP-7 is predicted to function as an anion transporter that regulates cellular pH and volume via transmembrane movement of electrolytes and fluids; a sulp-7::GFP transcriptional fusion is widely expressed in body wall, pharyngeal, and vulval muscles, head and body hypodermal cells, and the intestine.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 body wall musculature; hypodermis; intestine; pharyngeal muscle cell; and vulval muscle. Human ortholog(s) of this gene implicated in several diseases, including Pendred Syndrome; autosomal recessive nonsyndromic deafness (multiple); and bone disease (multiple). Is an ortholog of several human genes including SLC26A2 (solute carrier family 26 member 2); SLC26A3 (solute carrier family 26 member 3); and SLC26A4 (solute carrier family 26 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_model (15)
Molecular_infoCorresponding_CDSW04G3.6a
W04G3.6b
W04G3.6c
W04G3.6d
Corresponding_CDS_historyW04G3.6:wp131
W04G3.6:wp148
W04G3.9:wp131
Corresponding_transcriptW04G3.6a.1
W04G3.6b.1
W04G3.6c.1
W04G3.6d.1
Other_sequence (14)
Associated_featureWBsf648519
WBsf236348
WBsf236349
Experimental_infoRNAi_resultWBRNAi00054786Inferred_automaticallyRNAi_primary
WBRNAi00019604Inferred_automaticallyRNAi_primary
WBRNAi00019603Inferred_automaticallyRNAi_primary
WBRNAi00054785Inferred_automaticallyRNAi_primary
Expr_patternExpr3253
Expr1013550
Expr1158326
Expr2017118
Expr2035254
Drives_constructWBCnstr00011256
WBCnstr00030043
Construct_productWBCnstr00030043
Microarray_results (40)
Expression_cluster (74)
Interaction (11)
Map_infoMapXPosition2.85827
PositivePositive_cloneW04G3Inferred_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