MYB

MYB proto-oncogene, transcription factor
OMIM: 189990, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber MYB in Bone Marrow Failure


Level 2: Haematological disorders
Version 2.9

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • combined immunodeficiency, MONDO:0015131

    Amber MYB in Mendeliome


    Version 2.612

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • combined immunodeficiency, MONDO:0015131

    Amber MYB in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 2.10

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • combined immunodeficiency, MONDO:0015131