GAP43

growth associated protein 43
OMIM: 162060, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red GAP43 in Mendeliome


Version 1.2656

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • neurodevelopmental disorder, MONDO:0700092

Red GAP43 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.174

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • neurodevelopmental disorder, MONDO:0700092, GAP43-related