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WormBase Tree Display for Gene: WBGene00002150

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Name Class

WBGene00002150SMapS_parentSequenceM02A10
IdentityVersion1
NameCGC_nameirk-2Person_evidenceWBPerson655
Sequence_nameM02A10.2
Molecular_name (19)
Other_nameCELE_M02A10.2Accession_evidenceNDBBX284606
Public_nameirk-2
DB_infoDatabaseAceViewgeneXB322
WormQTLgeneWBGene00002150
WormFluxgeneWBGene00002150
NDBlocus_tagCELE_M02A10.2
PanthergeneCAEEL|WormBase=WBGene00002150|UniProtKB=A0A1C3NSN6
familyPTHR11767
NCBIgene191695
RefSeqproteinNM_001330888.3
NM_001270048.3
NM_001380895.1
NM_001380896.1
NM_001307921.4
NM_001270047.4
TrEMBLUniProtAccA0A1C3NSN6
H2KYE6
D3YT08
A0A1C3NSR3
U4PSB4
U4PN13
UniProt_GCRPUniProtAccA0A1C3NSN6
OMIMgene600681
600734
600937
613236
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classirk
Allele (166)
Legacy_information[Thomas JH] irk for Inward Rectifying potassium (K) channel family. Predicted gene M02A10.2
StrainWBStrain00037929
WBStrain00039809
WBStrain00047557
RNASeq_FPKM (74)
GO_annotation (14)
Ortholog (82)
ParalogWBGene00002149Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00002151Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionirk-2 encodes an inwardly rectifying potassium channel based on sequence homology to the the human potassium channel genes KCNJ1/KCNJ2.Paper_evidenceWBPaper00006402
Curator_confirmedWBPerson324
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable inward rectifier potassium channel activity. Predicted to be involved in potassium ion import across plasma membrane and regulation of monoatomic ion transmembrane transport. Predicted to be located in plasma membrane. Predicted to be part of monoatomic ion channel complex. Expressed in intestine; pharyngeal-intestinal valve cell; spermatheca; and uterus. Human ortholog(s) of this gene implicated in several diseases, including glucose metabolism disease (multiple); heart conduction disease (multiple); and long QT syndrome (multiple). Is an ortholog of several human genes including KCNJ2 (potassium inwardly rectifying channel subfamily J member 2); KCNJ4 (potassium inwardly rectifying channel subfamily J member 4); and KCNJ5 (potassium inwardly rectifying channel subfamily J member 5).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_model (16)
Molecular_infoCorresponding_CDSM02A10.2a
M02A10.2b
M02A10.2c
M02A10.2d
M02A10.2e
M02A10.2f
Corresponding_CDS_historyM02A10.2:wp204
M02A10.2b:wp239
Corresponding_transcriptM02A10.2a.1
M02A10.2a.2
M02A10.2b.1
M02A10.2c.1
M02A10.2d.1
M02A10.2e.1
M02A10.2f.1
Other_sequence (12)
Associated_featureWBsf1003844
WBsf1003845
WBsf1003846
WBsf1022163
WBsf236953
Experimental_infoRNAi_resultWBRNAi00050801Inferred_automaticallyRNAi_primary
WBRNAi00017113Inferred_automaticallyRNAi_primary
Expr_patternExpr16176
Expr16177
Expr16178
Expr1015830
Expr1154493
Expr2012824
Expr2031062
Drives_constructWBCnstr00036415
WBCnstr00042793
Construct_productWBCnstr00036415
WBCnstr00042793
Microarray_resultsSMD_M02A10.1
SMD_M02A10.2
187866_at
A_12_P101217
Aff_M02A10.2
GPL13394_WBGene00002150
GPL13914_M02A10.2
GPL14144_M02A10.2_647-706_0.881_20_B
GPL14144_M02A10.2_751-810_0.904_15_A
GPL14144_M02A10.2_941-1000_0.884_18_C
GPL19516_CGZ0029718
GPL19516_CGZ0029719
GPL19516_CGZ0029720
GPL19516_CGZ0029721
GPL21109_M02A10.2a
GPL3518_CE07387
GPL8304_CE_WBGene00002150_A
GPL8673_M02A10_2P00598
GPL8673_M02A10_2P00767
GPL8673_M02A10_2P01142
GPL9450_M02A10.2
cea2.i.55951
Expression_cluster (88)
Interaction (15)
Map_infoMapXPosition-19.5082
PositivePositive_cloneM02A10Person_evidenceWBPerson654
WBPerson655
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00006402
WBPaper00028146
WBPaper00034195
WBPaper00038491
WBPaper00055090
WBPaper00059550
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