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Protein-coding gene in humans
ATP-dependent potassium channel (Kir1.1) that in humans is encoded by the KCNJ1 gene. It plays an important role in potassium recycling in the thick ascending
KCNJ1
Medical condition
SLC12A1 (NKCC2) Na-K-2Cl symporter neonatal Bartter's syndrome type 2 ROMK/KCNJ1 thick ascending limb K+ channel classic Bartter's syndrome type 3 CLCNKB
Bartter_syndrome
Q9NS61 8007 KCNIP3 HGNC:15523; Q9Y2W7 8008 KCNIP4 HGNC:30083; Q6PIL6 8009 KCNJ1 HGNC:6255; P48048 8010 KCNJ2 HGNC:6263; P63252 8011 KCNJ3 HGNC:6264; P48549
List of human protein-coding genes 4
List_of_human_protein-coding_genes_4
Group of transmembrane proteins that passively transport potassium ions
Gene Protein Aliases Associated subunits KCNJ1 Kir1.1 ROMK1 NHERF2 KCNJ2 Kir2.1 IRK1 Kir2.2, Kir4.1, PSD-95, SAP97, AKAP79 KCNJ12 Kir2.2 IRK2 Kir2.1 and
Inward-rectifier potassium channel
Inward-rectifier_potassium_channel
Protein-coding gene in humans
channels: Epithelial Na+ channel ENaC Renal outer medullary K+ channel KCNJ1 (ROMK1) Renal epithelial Ca2+ channel TRPV5 Ubiquitous Cl− channel CLCN2
SGK1
Bartter syndrome, type 1; 601678; SLC12A1 Bartter syndrome, type 2; 241200; KCNJ1 Bartter syndrome, type 3; 607364; CLCNKB Bartter syndrome, type 4, digenic;
List_of_OMIM_disorder_codes
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KCNJ1
KCNJ1
KCNJ1
KCNJ1
KCNJ1
KCNJ1
KCNJ1
KCNJ1
KCNJ1
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