C15orf41

chromosome 15 open reading frame 41
OMIM: 615626, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green C15orf41 in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.123

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Eligibility statement prior genetic testing
  • UKGTN
Phenotypes
  • Dyserythropoietic anemia, congenital, type Ib, OMIM:615631
  • Congenital dyserythropoietic anemia type type 1B, MONDO:0014285
Tags
  • missense
  • new-gene-name
Green C15orf41 in Rare anaemia


Level 2: Haematology
Version 3.19
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • Dyserythropoietic anemia, congenital, type Ib, OMIM:615631
  • Congenital dyserythropoietic anemia type type 1B, MONDO:0014285
Tags
  • new-gene-name