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XB-GENEPAGE-983213
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???displayGene.symbol???: kcnj13
???displayGene.name???: potassium inwardly rectifying channel subfamily J member 13
???displayGene.synonyms???
kir7.1
(
???displayGene.geneFunction??? Inward rectifier K+ channel Protein Function
???displayGene.geneInteractants???
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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 | |||||||||||
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