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WormBase Tree Display for Gene: WBGene00003736

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Name Class

WBGene00003736SMapS_parentSequenceZK822
IdentityVersion1
NameCGC_namenhx-9
Sequence_nameZK822.3
Molecular_nameZK822.3a
ZK822.3a.1
CE27559
ZK822.3b
CE27560
ZK822.3c
CE28196
ZK822.3b.1
ZK822.3c.1
Other_nameCELE_ZK822.3Accession_evidenceNDBBX284604
Public_namenhx-9
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnhx
Allele (63)
StrainWBStrain00031663
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (49)
ParalogWBGene00003729Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003730Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003731Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00003732Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003733Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003734Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003735Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003943Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_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 excretory cell; intestine; and phasmid sensillum. 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_CDSZK822.3a
ZK822.3b
ZK822.3c
Corresponding_CDS_historyZK822.3:wp49
ZK822.3c:wp61
ZK822.3c:wp229
Corresponding_transcriptZK822.3a.1
ZK822.3b.1
ZK822.3c.1
Other_sequence (25)
Associated_featureWBsf216765
WBsf646433
WBsf646434
WBsf646435
WBsf660771
WBsf997992
WBsf229221
WBsf229222
Experimental_infoRNAi_resultWBRNAi00086174Inferred_automaticallyRNAi_primary
WBRNAi00059743Inferred_automaticallyRNAi_primary
WBRNAi00086173Inferred_automaticallyRNAi_primary
WBRNAi00059742Inferred_automaticallyRNAi_primary
Expr_patternExpr2238
Expr2248
Expr1014311
Expr1031747
Expr1163167
Expr2014260
Expr2032500
Drives_constructWBCnstr00010717
WBCnstr00010728
WBCnstr00035906
Construct_productWBCnstr00010728
WBCnstr00035906
Microarray_results (35)
Expression_cluster (165)
Interaction (29)
Map_infoMapIVPosition5.41637Error0.003754
PositivePositive_cloneZK822Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4302
Pseudo_map_position
ReferenceWBPaper00018859
WBPaper00035475
WBPaper00038491
WBPaper00047401
WBPaper00055090
WBPaper00064064
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