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WormBase Tree Display for Gene: WBGene00003730

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Name Class

WBGene00003730SMapS_parentSequenceB0495
IdentityVersion1
NameCGC_namenhx-2
Sequence_nameB0495.4
Molecular_nameB0495.4
B0495.4.1
CE48832
Other_nameCELE_B0495.4Accession_evidenceNDBBX284602
Public_namenhx-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnhx
Allele (34)
StrainWBStrain00035710
RNASeq_FPKM (74)
GO_annotation (35)
Ortholog (49)
ParalogWBGene00003729Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003736Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003733Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003735Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003731Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003943Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00003734Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00003732Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionnhx-2 encodes a sodium/proton exchanger; NHX-2 promotes normal peptide transporter function and recovery from intracellular acid load via catalysis of the electroneutral exchange of extracellular sodium for an intracellular proton; NHX-2 activity is required for normally high growth rates, and for propagation or maintenance of the germline; NHX-2 is expressed in the apical membranes of intestinal cells.Paper_evidenceWBPaper00005421
WBPaper00005654
WBPaper00006186
WBPaper00040287
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated21 Oct 2011 00:00:00
Automated_descriptionEnables sodium:proton antiporter activity. Involved in several processes, including determination of adult lifespan; positive regulation of growth rate; and regulation of transport. Located in apical plasma membrane. Expressed in intestine. Human ortholog(s) of this gene implicated in several diseases, including autosomal recessive spinocerebellar ataxia 19; 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:0080065Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11071)
DOID:6000Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11071)
DOID:0060777Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11073)
Molecular_infoCorresponding_CDSB0495.4
Corresponding_CDS_historyB0495.4:wp239
Corresponding_transcriptB0495.4.1
Other_sequence (11)
Associated_featureWBsf988538
WBsf988539
WBsf1012587
WBsf223370
Experimental_infoRNAi_result (40)
Expr_patternExpr113
Expr2233
Expr2241
Expr8046
Expr1020516
Expr1031742
Expr1143268
Expr2014254
Expr2032494
Drives_construct (47)
Construct_productWBCnstr00009193
WBCnstr00010721
WBCnstr00019888
WBCnstr00035911
AntibodyWBAntibody00002657
Microarray_results (18)
Expression_cluster (213)
Interaction (36)
Map_infoMapIIPosition0.523763Error0.005206
PositivePositive_cloneB0495Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4530
5562
Pseudo_map_position
Reference (26)
RemarkSequence connection from [Nehrke K, Melvin J]
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
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
MethodGene