The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: Gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism

K+ channels are essential for a variety of cellular functions in both excitable and nonexcitable cells, and K+ channel gene alteration has been recently described in cardiac and neurological disorders. To explore further the relations between hereditary human diseases and K+ channels, we isolated from a human cosmid library the gene encoding the inwardly rectifying K+ channel alpha-subunit Kir 2.2 (RCNJ12), PCR analysis performed on this clone indicates that the entire open reading frame is contained in one unique exon. A polymorphic (CA)(16) sequence was localized 2.2 kb upstream of the ATG start codon. Fluorescence in situ hybridization on human metaphases assigns the gene to band 17p11.1. The implication of a deletion of the Kir 2.2 gene in the Smith-Magenis syndrome, which is also localized at 17p11, is unlikely since a Kir 2.2-linked microsatellite sequence could be amplified from the DNA of a Smith-Magenis syndrome affected patient bearing a 17p interstitial deletion. (C) 1997 Academic Press