AGAP1

ArfGAP with GTPase domain, ankyrin repeat and PH domain 1
OMIM: 608651, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber AGAP1 in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.389

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Cerebral palsy, MONDO:0006497, AGAP1-related
Tags
  • SV/CNV

Amber AGAP1 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Cerebral palsy, MONDO:0006497, AGAP1-related