PanelApp (staging)
  1. Genes and Genomic Entities
  2. DCLRE1B

DCLRE1B

DNA cross-link repair 1B
OMIM: 609683, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green DCLRE1B in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.112

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Dyskeratosis congenita, autosomal recessive 8, MIM# 620133

    Green DCLRE1B in Mendeliome


    Version 1.2302

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dyskeratosis congenita, autosomal recessive 8, MIM# 620133

    Red DCLRE1B in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 1.114

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review Unknown
    Sources
    • Expert Review Red
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dyskeratosis congenita and Hoyeraal-Hreidarsson (HH) syndrome