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WormBase Tree Display for Gene: WBGene00008074

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Name Class

WBGene00008074SMapS_parentSequenceC43F9
IdentityVersion2
NameCGC_namenkb-2Person_evidenceWBPerson919
WBPerson287
Sequence_nameC43F9.6
Molecular_nameC43F9.6
C43F9.6.1
CE19734
Other_nameCELE_C43F9.6Accession_evidenceNDBBX284604
Public_namenkb-2
DB_infoDatabaseAceViewgene4L357
WormQTLgeneWBGene00008074
WormFluxgeneWBGene00008074
NDBlocus_tagCELE_C43F9.6
PanthergeneCAEEL|WormBase=WBGene00008074|UniProtKB=Q9XUG9
familyPTHR11523
NCBIgene177950
RefSeqproteinNM_069557.4
TrEMBLUniProtAccQ9XUG9
UniProt_GCRPUniProtAccQ9XUG9
OMIMgene182330
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
221 Oct 2008 09:57:22WBPerson2970Name_changeCGC_namenkb-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnkb
Allele (28)
StrainWBStrain00031380
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (54)
ParalogWBGene00007646Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010117Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable ATPase activator activity. Predicted to be involved in intracellular monoatomic cation homeostasis and monoatomic cation transmembrane transport. Predicted to be located in plasma membrane. Predicted to be part of sodium:potassium-exchanging ATPase complex. Human ortholog(s) of this gene implicated in several diseases, including atrophic gastritis; autoimmune gastritis; and essential hypertension. Is an ortholog of several human genes including ATP1B1 (ATPase Na+/K+ transporting subunit beta 1); ATP1B2 (ATPase Na+/K+ transporting subunit beta 2); and ATP1B3 (ATPase Na+/K+ transporting subunit beta 3).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:8929Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:820)
DOID:10825Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:804)
DOID:0040090Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:820)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:820)
Molecular_infoCorresponding_CDSC43F9.6
Corresponding_transcriptC43F9.6.1
Other_sequenceCJC18069_1
Associated_featureWBsf229005
Experimental_infoRNAi_resultWBRNAi00029767Inferred_automaticallyRNAi_primary
WBRNAi00011889Inferred_automaticallyRNAi_primary
WBRNAi00042391Inferred_automaticallyRNAi_primary
Expr_patternExpr1010637
Expr1146382
Expr2014269
Expr2032509
Drives_constructWBCnstr00033255
Construct_productWBCnstr00033255
Microarray_results (20)
Expression_cluster (171)
Interaction (271)
Map_infoMapIVPosition4.641Error0.000196
PositivePositive_cloneC43F9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00043657
WBPaper00065080
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