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WormBase Tree Display for Gene: WBGene00002151

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Name Class

WBGene00002151SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_nameirk-3Person_evidenceWBPerson655
Sequence_nameK04G11.5
Molecular_name (20)
Other_nameCELE_K04G11.5Accession_evidenceNDBBX284606
Public_nameirk-3
DB_infoDatabaseAceViewgeneXO970
WormQTLgeneWBGene00002151
WormFluxgeneWBGene00002151
NDBlocus_tagCELE_K04G11.5
PanthergeneCAEEL|WormBase=WBGene00002151|UniProtKB=A0A1C3NSK2
familyPTHR11767
NCBIgene191696
RefSeqproteinNM_001330918.4
NM_001330920.4
NM_001330921.5
NM_001392886.1
NM_001381146.1
NM_001330922.4
TrEMBLUniProtAccA0A1C3NSP8
Q93849
A0A1C3NSR4
A0A1C3NSS7
A0A1C3NSL2
A0A1C3NSK2
UniProt_GCRPUniProtAccA0A1C3NSK2
OMIMgene600359
602208
603208
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classirk
Allele (279)
Legacy_information[Thomas JH] irk for Inward Rectifying potassium (K) channel family. Predicted gene K04G11.5
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (56)
ParalogWBGene00002149Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00002150Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable inward rectifier potassium channel activity. Involved in short-term memory. Predicted to be located in plasma membrane. Predicted to be part of monoatomic ion channel complex. Expressed in HSNL; HSNR; and sensory neurons. Human ortholog(s) of this gene implicated in several diseases, including Bartter disease type 2; EAST syndrome; and Leber congenital amaurosis 16. Is an ortholog of human KCNJ10 (potassium inwardly rectifying channel subfamily J member 10); KCNJ13 (potassium inwardly rectifying channel subfamily J member 13); and KCNJ15 (potassium inwardly rectifying channel subfamily J member 15).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:0110498Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6256)
DOID:0060484Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6256)
DOID:0110143Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6255)
DOID:0111570Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6259)
DOID:0110118Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6259)
Molecular_infoCorresponding_CDSK04G11.5a
K04G11.5b
K04G11.5c
K04G11.5d
K04G11.5e
K04G11.5f
Corresponding_CDS_historyK04G11.5:wp83
K04G11.5:wp109
Corresponding_transcriptK04G11.5a.1
K04G11.5a.2
K04G11.5a.3
K04G11.5b.1
K04G11.5c.1
K04G11.5d.1
K04G11.5e.1
K04G11.5f.1
Other_sequence (17)
Associated_featureWBsf1007890
WBsf1007891
WBsf1007892
WBsf1007893
WBsf1024388
WBsf1024389
WBsf1024390
WBsf238234
Experimental_infoRNAi_resultWBRNAi00049930Inferred_automaticallyRNAi_primary
WBRNAi00033962Inferred_automaticallyRNAi_primary
WBRNAi00016608Inferred_automaticallyRNAi_primary
Expr_patternExpr16179
Expr1016162
Expr1153635
Expr2012825
Expr2031063
Drives_constructWBCnstr00036414
WBCnstr00042794
Construct_productWBCnstr00036414
Microarray_results (17)
Expression_cluster (125)
InteractionWBInteraction000214990
Map_infoMapXPosition16.6969
PositivePositive_cloneK04G11Person_evidenceWBPerson654
WBPerson655
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00034195
WBPaper00038491
WBPaper00048988
WBPaper00055090
WBPaper00064330
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