PanelApp
  1. Genes and Genomic Entities
  2. C15orf41

C15orf41

chromosome 15 open reading frame 41
OMIM: 615626, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green C15orf41 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.114

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Dyserythropoietic anemia, congenital, type Ib, MIM# 615631

    Green C15orf41 in Mendeliome


    Version 1.2374

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Dyserythropoietic anemia, congenital, type Ib, MIM# 615631

    Green C15orf41 in Red cell disorders


    Level 2: Haematological disorders
    Version 1.29

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    Phenotypes
    • Dyserythropoietic anaemia, congenital, type Ib, MIM# 615631

    Green C15orf41 in IBMDx study


    Version 0.35

    		review Unknown
    Sources
    • Expert Review Green
    • IBMDx Study
    • Expert Review Green
    • Expert list
    Phenotypes
    • Dyserythropoietic anemia, congenital, type Ib, MIM# 615631