GAP43

growth associated protein 43
OMIM: 162060, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

No list GAP43 in Mendeliome


Version 1.2511

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