XB-GENEPAGE-983213
???displayGene.symbol???:
kcnj13
???displayGene.name???:
potassium inwardly rectifying channel subfamily J member 13
???displayGene.synonyms???
kir7.1
(
Nomenclature history )
???displayGene.geneFunction???
Inward rectifier K+ channel
AI Protein Function
:
kcnj13 encodes an inward‑rectifier potassium channel (Kir7.1) that mediates potassium ion transport across the plasma membrane, regulates membrane potential, and supports pigment cell function; the pro...[+]
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Diseases:
Disease Ontology:
Leber congenital amaurosis 16
MIM:
VITREORETINAL DEGENERATION, SNOWFLAKE TYPE; SVD
External Links:
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