SORCS2

sortilin related VPS10 domain containing receptor 2
OMIM: 606284, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SORCS2 in Mendeliome


Version 1.3936

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, SORCS2-related

Red SORCS2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.325

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, SORCS2-related