ARAP3

ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3
OMIM: 606647, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red ARAP3 in Rare syndromic craniosynostosis or isolated multisuture synostosis


Level 2: Musculoskeletal
Version 6.3
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • craniosynostosis, MONDO:0015469
Amber ARAP3 in Primary lymphoedema


Level 2: Cardiology
Version 4.21
Latest signed off version: v4.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Lymphoedema, MONDO:0019297
Tags
  • watchlist