MYO5B

myosin VB
OMIM: 606540, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green MYO5B in Cholestasis


Level 2: Gastroenterological disorders
Version 0.240

Component of the following Super Panels:

  • Liverome Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Cholestasis
    • Microvillus inclusion disease, MIM#251850

    Green MYO5B in Congenital Diarrhoea


    Level 2: Gastroenterological disorders
    Version 1.13

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Microvillus inclusion disease, MIM# 251850

    Green MYO5B in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Microvillus inclusion disease, MIM# 251850
    • Cholestasis

    Green MYO5B in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Microvillus inclusion disease, 251850 (3)

    Green MYO5B in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Microvillus inclusion disease, 251850 (3)

    Green MYO5B in Prepair 500+


    Level 2: Screening
    Version 1.1

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Microvillus inclusion disease, 251850 (3)