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KCNJ5

potassium inwardly rectifying channel subfamily J member 5

HCNC Approved Symbol
KCNJ5 (HGNC:6266)
Genomic Coordinates
11:128,891,356 - 128,921,163 (11q24.3)
Synonyms
Kir3.4, CIR, KATP1, GIRK4, LQT13
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Hyperaldosteronism, familial, type III
613677AD
Long QT syndrome 13
613485AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the KCNJ5 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results