C17orf62

chromosome 17 open reading frame 62
Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Amber C17orf62 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.121

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert Review
    Phenotypes
    • Chronic granulomatous disease

    Green C17orf62 in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Chronic granulomatous disease 5, autosomal recessive, MIM# 618935
    Tags
    • new gene name

    Green C17orf62 in Phagocyte Defects


    Level 2: Immunological disorders
    Version 1.29

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Expert Review Green
    • Expert list
    Phenotypes
    • Chronic granulomatous disease 5, autosomal recessive, MIM# 618935
    Tags
    • new gene name

    Green C17orf62 in Chronic granulomatous disease


    Level 2: Immunological disorders
    Version 1.3

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Chronic granulomatous disease
    Tags
    • new gene name

    Green C17orf62 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Chronic granulomatous disease 5, autosomal recessive, MIM# 618935
    Tags
    • new gene name
    • treatable
    • immunological