KCNQ2 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description potassium channel, voltage gated KQT-like subfamily Q, member 2|The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 3785)
External Link http://www.ncbi.nlm.nih.gov/gene/3785
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Genes

5 interacting proteins for KCNQ2 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
ARIH2 ariadne RBR E3 ubiquitin protein ligase 2
CALM1 calmodulin 1 (phosphorylase kinase, delta)
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
PRKCA protein kinase C, alpha