C15orf41

chromosome 15 open reading frame 41
OMIM: 615626, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green C15orf41 in Cytopenias and congenital anaemias Level 3: Anaemias and red cell disorders Level 2: Haematological disorders Version 1.118	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 3.8 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
Green C15orf41 in Severe Paediatric Disorders Version 1.184	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