SV2A:Ensemblv115

synaptic vesicle glycoprotein 2A
OMIM: 185860, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber SV2A in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, SV2A-related
  • Developmental and epileptic encephalopathy 113, MIM# 620772