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WormBase Tree Display for Gene: WBGene00003570

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Name Class

WBGene00003570SMapS_parentSequenceCHROMOSOME_V
IdentityVersion1
NameCGC_namencx-5
Sequence_nameY32F6B.2
Molecular_nameY32F6B.2
Y32F6B.2.1
CE42032
Other_nameCELE_Y32F6B.2Accession_evidenceNDBBX284605
Public_namencx-5
DB_infoDatabaseAceViewgene5K964
WormQTLgeneWBGene00003570
WormFluxgeneWBGene00003570
NDBlocus_tagCELE_Y32F6B.2
PanthergeneCAEEL|WormBase=WBGene00003570|UniProtKB=G5EC02
familyPTHR10846
NCBIgene191715
RefSeqproteinNM_073289.4
TrEMBLUniProtAccG5EC02
UniProt_GCRPUniProtAccG5EC02
OMIMgene603617
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classncx
Allele (59)
Legacy_information[Kraev A] ncx for Na/Ca eXchanger. No mutants known. See ncx-1. Predicted gene Y36F6B.2 (incomplete)
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (36)
ParalogWBGene00003569Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionncx-5 encodes a putative 4Na[+]/1Ca[2+],1K[+] exchanger, orthologous tohuman SLC24A1-5 and paralogous to NCX-4; NCX-5 is predicted to exportfree cytoplasmic Ca[2+] with low affinity but high capacity, beingcomplemented by low-capacity/high-affinity Ca[2+] ATPase pumps such asMCA-1/-3; NCX-5 has tandem Calx-alpha domains predicted to carry out iontransport; NCX-5 has no obvious function in mass RNAi assays.Paper_evidenceWBPaper00012774
WBPaper00028596
WBPaper00031156
WBPaper00031157
WBPaper00031158
Curator_confirmedWBPerson567
Date_last_updated07 Nov 2007 00:00:00
Automated_descriptionPredicted to enable calcium channel activity and calcium, potassium:sodium antiporter activity. Predicted to be involved in calcium ion transmembrane transport and intracellular calcium ion homeostasis. Predicted to be located in membrane. Expressed in oxygen sensory neurons. Human ortholog(s) of this gene implicated in congenital stationary night blindness 1D. Is an ortholog of human SLC24A1 (solute carrier family 24 member 1) and SLC24A2 (solute carrier family 24 member 2).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:0110868Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10975)
Molecular_infoCorresponding_CDSY32F6B.2
Corresponding_CDS_historyY32F6B.2:wp186
Corresponding_transcriptY32F6B.2.1
Other_sequenceSS01991
JI171836.1
Oden_isotig28524
SSC00546_1
Associated_featureWBsf1001123
Experimental_infoRNAi_resultWBRNAi00055788Inferred_automaticallyRNAi_primary
WBRNAi00055789Inferred_automaticallyRNAi_primary
Expr_patternExpr11159
Expr1018301
Expr1159321
Expr2013922
Expr2032162
Drives_constructWBCnstr00018019
WBCnstr00036035
Construct_productWBCnstr00036035
Microarray_results (16)
Expression_cluster (64)
Interaction (18)
Map_infoMapVPosition2.56961Error0.000102
PositivePositive_cloneY32F6Author_evidenceKraev A
Y32F6BInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00060661
WBPaper00062223
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