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WormBase Tree Display for Gene: WBGene00003731

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Name Class

WBGene00003731SMapS_parentSequenceC54F6
IdentityVersion1
NameCGC_namenhx-3
Sequence_nameC54F6.13
Molecular_nameC54F6.13a
C54F6.13a.1
CE32044
C54F6.13b
CE08985
C54F6.13a.2
C54F6.13b.1
Other_nameCELE_C54F6.13Accession_evidenceNDBBX284605
Public_namenhx-3
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnhx
AlleleWBVar01741223
WBVar01484282
WBVar01499740
WBVar01500129
WBVar01499056
WBVar01974191
WBVar00462805
WBVar00462806
WBVar00462807
WBVar00462808
WBVar00462809
WBVar00093141
WBVar00462810
WBVar01025528
WBVar01025529
WBVar01025530
WBVar01025531
WBVar01025532
WBVar01025533
WBVar01025534
WBVar01025535
WBVar00092319
WBVar01025536
WBVar01025537
WBVar01025538
WBVar01025539
WBVar01025540
WBVar01025541
WBVar00212031
WBVar01025542
WBVar00212032
WBVar01025543
WBVar00212033
WBVar01025544
WBVar01025545
WBVar01025546
WBVar01025547
WBVar01025548
WBVar01025549
WBVar00264383
WBVar01025550
WBVar01025551
WBVar01025552
WBVar01025553
WBVar01651968
WBVar01025554
WBVar01025555
WBVar01025556
WBVar00067449
WBVar01025557
WBVar02136625
WBVar01499496
WBVar01499316
WBVar01822082
WBVar01500066
WBVar00249880
StrainWBStrain00036007
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (53)
ParalogWBGene00003729Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003730Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003736Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00003733Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003735Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003943Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003734Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003732Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionnhx-3 encodes a sodium/proton exchanger expressed intracellularly (in elliptical, randomly distributed dots that might be multivesicular or Ward bodies) within hypodermal cells of the main body syncytium, socket cells, and the excretory pore cell, as well as (in adults) within uterine cells (probably ut1) in the region closest to the vulva, in spermathecal junction cells; nhx-3 has no obvious phenotype in mass RNAi screens; NHX-3 is thought to prevent intracellular acidification by catalysing the electroneutral exchange of vesicular sodium for an intracellular proton; speculatively, NHX-3 might enable hypodermis-specific secretion of cuticle or phagocytosis.Paper_evidenceWBPaper00005421
WBPaper00005654
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable potassium:proton antiporter activity and sodium:proton antiporter activity. Predicted to be involved in potassium ion transmembrane transport; regulation of intracellular pH; and sodium ion import across plasma membrane. Predicted to be located in plasma membrane. Expressed in epithelial cell; hypodermis; and spermathecal-uterine junction. Human ortholog(s) of this gene implicated in congenital secretory sodium diarrhea 8 and end stage renal disease. Is an ortholog of human SLC9A3 (solute carrier family 9 member A3) and SLC9A5 (solute carrier family 9 member A5).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:783Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11078)
DOID:0060777Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11073)
Molecular_infoCorresponding_CDSC54F6.13a
C54F6.13b
Corresponding_CDS_historyC54F6.13:wp87
Corresponding_transcriptC54F6.13a.1
C54F6.13a.2
C54F6.13b.1
Other_sequence (12)
Associated_featureWBsf652778
WBsf233955
Experimental_infoRNAi_resultWBRNAi00030150Inferred_automaticallyRNAi_primary
WBRNAi00107732Inferred_automaticallyRNAi_primary
WBRNAi00107733Inferred_automaticallyRNAi_primary
WBRNAi00043163Inferred_automaticallyRNAi_primary
WBRNAi00012401Inferred_automaticallyRNAi_primary
WBRNAi00115930Inferred_automaticallyRNAi_primary
Expr_patternExpr2236
Expr2245
Expr1013171
Expr1147139
Expr2014255
Expr2032495
Drives_constructWBCnstr00010715
WBCnstr00010725
WBCnstr00035910
Construct_productWBCnstr00010725
WBCnstr00035910
Microarray_results (22)
Expression_cluster (129)
Interaction (16)
Map_infoMapVPosition0.773277Error0.003626
PositivePositive_cloneC54F6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5336
5364
Pseudo_map_position
ReferenceWBPaper00032165
WBPaper00038491
WBPaper00049246
WBPaper00055090
WBPaper00065561
RemarkSequence connection from [Nehrke K, Melvin J]
nxh-2 nxh-3 nxh-4 nxh-5 nxh-6 nxh-7 nxh-8 nxh-9 published in cgc5421 actually refer to nhx genesCGC_data_submission
Map 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