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WormBase Tree Display for Gene: WBGene00001137

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Name Class

WBGene00001137SMapS_parentSequenceB0365
IdentityVersion1
NameCGC_nameeat-6Person_evidenceWBPerson32
Sequence_nameB0365.3
Molecular_nameB0365.3
B0365.3.1
CE07721
B0365.3.2
Other_nameNaK/1
spa-1
CELE_B0365.3Accession_evidenceNDBBX284605
Public_nameeat-6
DB_infoDatabaseAceViewgene5N608
WormQTLgeneWBGene00001137
WormFluxgeneWBGene00001137
NDBlocus_tagCELE_B0365.3
PanthergeneCAEEL|WormBase=WBGene00001137|UniProtKB=P90735
familyPTHR43294
NCBIgene179796
RefSeqproteinNM_073868.6
TrEMBLUniProtAccP90735
UniProt_GCRPUniProtAccP90735
OMIMgene182310
182340
182350
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classeat
Allele (46)
Legacy_information (3)
StrainWBStrain00036106
WBStrain00037778
WBStrain00005464
WBStrain00005489
WBStrain00005507
WBStrain00005516
WBStrain00005529
RNASeq_FPKM (74)
GO_annotation (36)
Ortholog (46)
Paralog (14)
Structured_descriptionConcise_descriptioneat-6 encodes an ortholog of the alpha subunit of a sodium/potassium ATPase, which in turn affects Na+,K(+)-ATPase activity of membranes by affecting the level of the phosphorylated intermediate of the Na+,K(+)-ATPase; EAT-6 affects relaxation of the pharyngeal muscles, fertility (and thus affects feeding); EAT-6 also affects body length, life span, and ASE, ASI and ASJ axonal outgrowth.Paper_evidenceWBPaper00001709
WBPaper00002371
WBPaper00003150
WBPaper00003257
WBPaper00003521
Curator_confirmedWBPerson48
WBPerson363
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables P-type sodium:potassium-exchanging transporter activity. Involved in several processes, including action potential; monoatomic ion transport; and regulation of muscle contraction. Located in membrane. Expressed in several structures, including coelomocyte; intestine; neurons; pharynx; and vulval muscle. Used to study alcohol use disorder. Human ortholog(s) of this gene implicated in several diseases, including Charcot-Marie-Tooth disease type 2DD; alternating hemiplegia of childhood; and brain disease (multiple). Is an ortholog of human ATP1A3 (ATPase Na+/K+ transporting subunit alpha 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_infoExperimental_modelDOID:1574Homo sapiensPaper_evidenceWBPaper00045914
Curator_confirmedWBPerson324
Date_last_updated06 Jun 2019 00:00:00
Potential_model (12)
Models_disease_assertedWBDOannot00000704
Molecular_infoCorresponding_CDSB0365.3
Corresponding_transcriptB0365.3.1
B0365.3.2
Other_sequence (276)
Associated_feature (18)
Experimental_infoRNAi_result (34)
Expr_patternExpr8226
Expr8228
Expr12845
Expr1017676
Expr1030726
Expr1143152
Expr2011160
Expr2029396
Drives_constructWBCnstr00013194
WBCnstr00022897
WBCnstr00037068
Construct_productWBCnstr00013192
WBCnstr00037068
Microarray_results (26)
Expression_cluster (174)
Interaction (116)
Map_infoMapVPosition4.93766Error0.013547
Well_ordered
PositivePositive_cloneB0365Inferred_automaticallyFrom sequence, transcript, pseudogene data
DF#NK1
R07B8
Mapping_data2_point5213
Multi_point1837
1839
1840
1841
2403
2404
3844
4482
Pos_neg_data (4)
Reference (55)
Remark[MW Davis] Transformation rescue.
MethodGene