# Potassium voltage-gated channel subfamily Q member 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q6449561](https://www.wikidata.org/wiki/Q6449561)  
**Source**: https://4ort.xyz/entity/potassium-voltage-gated-channel-subfamily-q-member-2-q6449561


## References

1. UniProt
2. IUPHAR/BPS Guide to PHARMACOLOGY
3. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O43526)
4. Q20641742
5. [A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
7. [Structural Insights into the M-Channel Proximal C-Terminus/Calmodulin Complex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
8. [KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
10. [Structural Insights into the M-Channel Proximal C-Terminus/Calmodulin Complex](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43526&geneProductId=UniProtKB:O43526)
11. [A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43526&geneProductId=UniProtKB:O43526)
12. [Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
13. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43526&geneProductId=UniProtKB:O43526)
14. [KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43526&geneProductId=UniProtKB:O43526)
15. [A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43526)
16. Ensembl Release 99
17. UMLS 2023
18. Transporter Classification database