Symbol
| KCNQ2
| contributors: mct - updated : 27-09-2011
|
HGNC name
| potassium voltage-gated channel, KQT-like subfamily, member 2
|
HGNC id
| 6296
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --low
|  
|
substantial downregulation of its expression in neuropathic injury | |
Susceptibility
|
to idiopathic epilepsy |
Variant & Polymorphism
SNP
| missense variant p.Pro574Ser detected in idiopathic epilepsy |
|
|
Candidate gene
Marker
Therapy target
| | | |