RASA2

RAS p21 protein activator 2
OMIM: 601589, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red RASA2 in Pigmentary skin disorders


Version 1.9
Latest signed off version: v1.4 (15 Oct 2020)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Other
Phenotypes
  • Noonan syndrome?

Amber RASA2 in RASopathies

Level 3: RASopathies
Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.75

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • Noonan syndrome?

Amber RASA2 in Cardiomyopathies - including childhood onset


Version 1.19
Latest signed off version: v1.4 (19 Feb 2020)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • NHS GMS
  • London South GLH
Phenotypes
  • Noonan syndrome?