KCNQ2
HGNC:6296 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in KCNQ2 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| epilepsy | HP:0001250 | 3 | 3 |
| developmental delay | HP:0001263 | 1 | 1 |
Linked variants
Variants normalized to KCNQ2| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | 1 | 1 |
| Saudi Arabia | — | 45 | 1 |
Supporting publications
3 records- 2023Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital.Children (Basel, Switzerland)PubMed ↗
- 2015Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy.CNS & neurological disorders drug targetsPubMed ↗
- 2012Frontal motor seizure following non-convulsive status epilepticus in ring chromosome 20 syndrome.Neurosciences (Riyadh, Saudi Arabia)PubMed ↗