Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00017464

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00017464SMapS_parentSequenceF14D12
IdentityVersion2
NameCGC_namesulp-2Person_evidenceWBPerson2233
Sequence_nameF14D12.5
Molecular_nameF14D12.5
F14D12.5.1
CE27963
Other_nameCELE_F14D12.5Accession_evidenceNDBBX284606
Public_namesulp-2
DB_infoDatabaseAceViewgeneXG216
WormQTLgeneWBGene00017464
WormFluxgeneWBGene00017464
NDBlocus_tagCELE_F14D12.5
PanthergeneCAEEL|WormBase=WBGene00017464|UniProtKB=G5EDS5
familyPTHR11814
NCBIgene180828
RefSeqproteinNM_076543.7
TrEMBLUniProtAccG5EDS5
UniProt_GCRPUniProtAccG5EDS5
OMIMgene126650
604943
605646
610130
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 Jan 2005 16:30:54WBPerson2970Name_changeCGC_namesulp-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsulp
AlleleWBVar00092761Inferred_automaticallyFrom strain object: RB1366
WBVar00092764Inferred_automaticallyFrom strain object: RB1369
WBVar01468992
WBVar01468993
WBVar01879611
WBVar01879612
WBVar01468994
WBVar02050592
WBVar01879613
WBVar01468997
WBVar01879614
WBVar00504124
WBVar00504125
WBVar00504126
WBVar00504127
WBVar00504128
WBVar00504129
WBVar01819953
WBVar00079236
WBVar01148530
WBVar00079237
WBVar00079238
WBVar01148531
WBVar00079239
WBVar01148532
WBVar00079240
WBVar01148533
WBVar00079241
WBVar01148534
WBVar01148535
WBVar01148536
WBVar01148537
WBVar01148538
WBVar01148539
WBVar01148540
WBVar01148541
WBVar01148542
WBVar01148543
WBVar01148544
WBVar01148545
WBVar01148546
WBVar01148547
WBVar01148548
WBVar01148549
WBVar01148550
WBVar01148551
WBVar01830573
WBVar02063882
WBVar01549994
WBVar01500067
StrainWBStrain00032065
WBStrain00032068
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (44)
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
WBGene00018283Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020914Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionsulp-2 encodes one of eight C. elegans members of the sulfate permease family of anion transporters; by homology, SULP-2 is predicted to function as an anion transporter that regulates cellular pH and volume via transmembrane movement of electrolytes and fluids and when expressed in Xenopus oocytes, SULP-2 does exhibit modest uptake of sulfate; a SULP-2::GFP fusion is expressed in the intestine and rectal gland cells, where it localizes to the basolateral membrane and in cephalic and deirid neurons, where it localizes to sensillar endings.Paper_evidenceWBPaper00025075
Curator_confirmedWBPerson1843
Date_last_updated13 Sep 2006 00:00:00
Automated_descriptionEnables sulfate transmembrane transporter activity. Predicted to be involved in inorganic anion transmembrane transport and organic anion transport. Located in basolateral plasma membrane and non-motile cilium. Expressed in dopaminergic neurons and intestine. Human ortholog(s) of this gene implicated in several diseases, including Pendred Syndrome; autosomal recessive nonsyndromic deafness (multiple); and calcium oxalate nephrolithiasis. Is an ortholog of several human genes including SLC26A1 (solute carrier family 26 member 1); 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_modelDOID:12176Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8818)
DOID:0060744Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8818)
DOID:0060296Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3018)
DOID:0110498Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8818)
DOID:0110513Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9359)
DOID:0080652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10993)
DOID:13250Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3018)
Molecular_infoCorresponding_CDSF14D12.5
Corresponding_transcriptF14D12.5.1
Other_sequenceCJC12795_1
Associated_featureWBsf670538
WBsf237387
Experimental_infoRNAi_resultWBRNAi00000992Inferred_automaticallyRNAi_primary
WBRNAi00030931Inferred_automaticallyRNAi_primary
WBRNAi00013264Inferred_automaticallyRNAi_primary
WBRNAi00044586Inferred_automaticallyRNAi_primary
Expr_patternExpr3247
Expr3259
Expr1010356
Expr1148543
Expr2017113
Expr2035249
Drives_constructWBCnstr00011250
WBCnstr00011262
WBCnstr00027278
Construct_productWBCnstr00011262
WBCnstr00027278
Microarray_results (18)
Expression_cluster (152)
Interaction (24)
Map_infoMapXPosition-4.46315Error0.008938
PositivePositive_cloneF14D12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5231
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