HGNC:6407

GPTKB entity

Statements (87)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alias gptkb:ATFB10
gptkb:CMH9
gptkb:HHBIRK1
gptkb:HHIRK1
gptkb:IRK-1
gptkb:KCNJ2*1
gptkb:KCNJ2*10
gptkb:KCNJ2*11
gptkb:KCNJ2*12
gptkb:KCNJ2*13
gptkb:KCNJ2*14
gptkb:KCNJ2*15
gptkb:KCNJ2*16
gptkb:KCNJ2*17
gptkb:KCNJ2*18
gptkb:KCNJ2*19
gptkb:KCNJ2*2
gptkb:KCNJ2*20
gptkb:KCNJ2*21
gptkb:KCNJ2*22
gptkb:KCNJ2*23
gptkb:KCNJ2*25
gptkb:KCNJ2*26
gptkb:KCNJ2*27
gptkb:KCNJ2*28
gptkb:KCNJ2*29
gptkb:KCNJ2*3
gptkb:KCNJ2*31
gptkb:KCNJ2*32
gptkb:KCNJ2*33
gptkb:KCNJ2*37
gptkb:KCNJ2*39
gptkb:KCNJ2*40
gptkb:KCNJ2*41
gptkb:KCNJ2*42
gptkb:KCNJ2*44
gptkb:KCNJ2*46
gptkb:KCNJ2*47
gptkb:KCNJ2*48
gptkb:KCNJ2*5
gptkb:KCNJ2*50
gptkb:KCNJ2*6
gptkb:KCNJ2*7
gptkb:KCNJ2*8
gptkb:KCNJ2*9
gptkb:KIR2.1
gptkb:LQT7
gptkb:SQT3
gptkb:hIRK1
KCNJ2*24
KCNJ2*30
KCNJ2*34
KCNJ2*35
KCNJ2*36
KCNJ2*38
KCNJ2*4
KCNJ2*43
KCNJ2*45
KCNJ2*49
gptkbp:approvedBy gptkb:potassium_inwardly_rectifying_channel_subfamily_J_member_2
gptkbp:approvedSymbol gptkb:KCNJ2
gptkbp:associatedWith gptkb:Andersen-Tawil_syndrome
gptkb:Familial_atrial_fibrillation
gptkb:Long_QT_syndrome_7
gptkb:Short_QT_syndrome_3
gptkbp:Entrez_Gene_ID 3759
ENSG00000104435
https://www.w3.org/2000/01/rdf-schema#label HGNC:6407
gptkbp:locatedOnChromosome 17
gptkbp:location 17q24.3
gptkbp:locusType gptkb:gene
gene with protein product
gptkbp:OMIM 600681
gptkbp:previousName gptkb:inward_rectifier_potassium_channel_1
gptkb:potassium_channel,_inwardly_rectifying_subfamily_J,_member_2
gptkbp:previousSymbols gptkb:IRK1
gptkb:KIR2.1
gptkbp:proteinFamily gptkb:inwardly_rectifying_potassium_channels
gptkb:potassium_channels
gptkbp:RefSeq NM_000891
gptkbp:species gptkb:Homo_sapiens
gptkbp:ucscId uc002hyn.4
gptkbp:UniProtID P63252
gptkbp:vegaId OTTHUMG00000150113
gptkbp:bfsParent gptkb:KRAS
gptkbp:bfsLayer 5