PanelApp (test)
  1. Genes and Genomic Entities
  2. IL21:Ensemblv90

IL21:Ensemblv90

interleukin 21
OMIM: 605384, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Red IL21 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.126

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert Review
    Phenotypes
    • Immunodeficiency, common variable, 11, MIM# 615767

    Red IL21 in Mendeliome


    Version 1.3802

    		3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review
    • Expert Review Red
    • Literature
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency, common variable, 11, MIM# 615767

    Red IL21 in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 1.138

    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
    • Immunodeficiency, common variable, 11, MIM# 615767

    Red IL21 in Common Variable Immunodeficiency


    Level 2: Immunological disorders
    Version 1.15

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Immunodeficiency, common variable, 11 MIM#615767

    Red IL21 in Inflammatory bowel disease


    Level 2: Gastroenterological disorders
    Version 1.0

    		3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review
    • Expert Review Red
    Phenotypes
    • Immunodeficiency, common variable, 11, MIM# 615767

    Red IL21 in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 2.0

    		1 review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Expert Review Red
    Phenotypes
    • Immunodeficiency, common variable, 11, MIM# 615767

    Red IL21 in Common Variable Immunodeficiency


    Level 2: Immunological disorders
    Version 2.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Red
    Phenotypes
    • Immunodeficiency, common variable, 11 MIM#615767