XB-GENEPAGE-483959
???displayGene.symbol???:
kcnj1
???displayGene.name???:
potassium inwardly rectifying channel subfamily J member 1
???displayGene.synonyms???
kir1.1
,
MGC68935
,
ROMK
,
romk1
(
Nomenclature history )
???displayGene.geneFunction???
potassium channel
AI Protein Function
:
kcnj1 encodes an inward‑rectifier potassium channel (Kir1.1) that functions as a membrane‑bound ion channel mediating potassium reabsorption; the protein localizes to the basolateral plasma membrane of...[+]
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
Bartter disease type 1
MIM:
BARTTER SYNDROME, TYPE 2, ANTENATAL; BARTS2
External Links:
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| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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Symbol legend:
