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XB-GENEPAGE-983213
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 kcnj13

???displayGene.name???: 
potassium inwardly rectifying channel subfamily J member 13

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kir7.1 ( Nomenclature history )

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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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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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