RHAG

Rh associated glycoprotein
OMIM: 180297, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green RHAG in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Anaemia, haemolytic, Rh-null, regulator type MIM# 268150
  • Overhydrated hereditary stomatocytosis MIM#185000

Red RHAG in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Rh-deficiency syndrome

Green RHAG in Red cell disorders


Level 2: Haematological disorders
Version 1.24

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Yorkshire and North East GLH
  • NHS GMS
  • Wessex and West Midlands GLH
  • North West GLH
  • London South GLH
Phenotypes
  • Anaemia, haemolytic, Rh-null, regulator type MIM# 268150
  • Overhydrated hereditary stomatocytosis MIM#185000

Red RHAG in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Rh-deficiency syndrome