BPGM

bisphosphoglycerate mutase
OMIM: 613896, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green BPGM in Mendeliome


Version 1.4852

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Erythrocytosis, familial, 8, MIM# 222800

Red BPGM in Additional findings_Paediatric


Level 2: Screening
Version 0.280

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Erythrocytosis due to bisphosphoglycerate mutase deficiency

Green BPGM in Red cell disorders


Level 2: Haematological disorders
Version 1.57

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Erythrocytosis, familial, 8, MIM# 222800

Red BPGM in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.148

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Erythrocytosis due to bisphosphoglycerate mutase deficiency