# Potassium inwardly rectifying channel subfamily J member 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q2004050](https://www.wikidata.org/wiki/Q2004050)  
**Source**: https://4ort.xyz/entity/potassium-inwardly-rectifying-channel-subfamily-j-member-2


## References

1. UniProt
2. Q20641742
3. [Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
5. [Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P63252&geneProductId=UniProtKB:P63252)
7. [Direct and Specific Activation of Human Inward Rectifier K+ Channels by Membrane Phosphatidylinositol 4,5-Bisphosphate](http://www.ebi.ac.uk/QuickGO/annotations?protein=P63252&geneProductId=UniProtKB:P63252)
8. [Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=P63252&geneProductId=UniProtKB:P63252)
9. [Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies](http://www.ebi.ac.uk/QuickGO/annotations?protein=P63252&geneProductId=UniProtKB:P63252)
10. [Direct and Specific Activation of Human Inward Rectifier K+ Channels by Membrane Phosphatidylinositol 4,5-Bisphosphate](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
11. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
12. [Molecular cloning and expression of a human heart inward rectifier potassium channel](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
13. [Inwardly rectifying potassium channels: their structure, function, and physiological roles](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
14. [A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P63252)
15. Ensembl Release 99
16. Identifiers.org
17. Transporter Classification database