# Potassium inwardly rectifying channel subfamily J member 11

> mammalian protein found in Homo sapiens

**Wikidata**: [Q6414726](https://www.wikidata.org/wiki/Q6414726)  
**Source**: https://4ort.xyz/entity/potassium-inwardly-rectifying-channel-subfamily-j-member-11


## References

1. UniProt
2. IUPHAR/BPS Guide to PHARMACOLOGY
3. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL498)
4. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1272)
5. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL783)
6. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL471498)
7. Q20641742
8. [Ankyrin-B regulates Kir6.2 membrane expression and function in heart](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
9. [Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
11. [Dual role of K ATP channel C-terminal motif in membrane targeting and metabolic regulation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
12. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
13. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14654&geneProductId=UniProtKB:Q14654)
14. [Molecular mechanism for ATP-dependent closure of the K+ channel Kir6.2](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
15. [The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
16. [Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
17. [Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14654)
18. Ensembl Release 99
19. Transporter Classification database