C15orf41

chromosome 15 open reading frame 41
OMIM: 615626, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green C15orf41 in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.88

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


Version 1.29
Latest signed off version: v1.2 (3 Mar 2020)

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

Green C15orf41 in Severe Paediatric Disorders


Version 1.84

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Dyserythropoietic anemia, congenital, type Ib, OMIM:615631
  • Congenital dyserythropoietic anemia type type 1B, MONDO:0014285
Tags
  • new-gene-name