# Potassium voltage-gated channel subfamily C member 3

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21107880](https://www.wikidata.org/wiki/Q21107880)  
**Source**: https://4ort.xyz/entity/potassium-voltage-gated-channel-subfamily-c-member-3


## References

1. UniProt
2. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL821)
3. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q14003)
4. Q20641742
5. [KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14003&geneProductId=UniProtKB:Q14003)
6. [Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14003&geneProductId=UniProtKB:Q14003)
7. [Spinocerebellar ataxia-13 Kv3.3 potassium channels: arginine-to-histidine mutations affect both functional and protein expression on the cell surface](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14003&geneProductId=UniProtKB:Q14003)
8. [Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14003&geneProductId=UniProtKB:Q14003)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q14003&geneProductId=UniProtKB:Q14003)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
11. [Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
12. [KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
13. [Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
14. [Spinocerebellar ataxia-13 Kv3.3 potassium channels: arginine-to-histidine mutations affect both functional and protein expression on the cell surface](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
15. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
16. [KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q14003)
17. Ensembl Release 99
18. Transporter Classification database