HGNC:6252

URI: https://gptkb.org/entity/HGNC:6252

GPTKB entity

Predicate	Object
gptkbp:instanceOf	gptkb:Ensembl_gene_ID
gptkbp:alias	gptkb:ATFB10 gptkb:IRK1 gptkb:KIR2.1 gptkb:HH gptkb:HHB
gptkbp:approvedBy	gptkb:potassium_inwardly_rectifying_channel_subfamily_J_member_2
gptkbp:approvedSymbol	gptkb:KCNJ2
gptkbp:associatedWith	gptkb:Andersen-Tawil_syndrome gptkb:Long_QT_syndrome_7 gptkb:Kir2.1
gptkbp:Entrez_Gene_ID	3759 ENSG00000143603
gptkbp:fullName	gptkb:potassium_inwardly_rectifying_channel_subfamily_J_member_2
gptkbp:gene	gptkb:KCNJ2
gptkbp:geneType	protein-coding
gptkbp:HGNC_ID	gptkb:HGNC:6252
gptkbp:locatedOnChromosome	17
gptkbp:locusType	17q24.3
gptkbp:OMIM	600681
gptkbp:organism	gptkb:Homo_sapiens
gptkbp:refersTo	gptkb:KCNJ2
gptkbp:UniProtID	P63252
gptkbp:bfsParent	gptkb:potassium_inwardly_rectifying_channel_subfamily_J_member_2
gptkbp:bfsLayer	7
http://www.w3.org/2000/01/rdf-schema#label	HGNC:6252