Kir6.2
From Wikipedia, the free encyclopedia
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potassium inwardly-rectifying channel, subfamily J, member 11
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| Identifiers | |
| Symbol | KCNJ11 |
| HUGO | 6257 |
| Entrez | 3767 |
| OMIM | 600937 |
| RefSeq | NM_000525 |
| UniProt | Q14654 |
| Other data | |
| Locus | Chr. 11 p15.1 |
Kir6.2 is a gene associated with congenital hyperinsulinism.
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