TLR8

toll like receptor 8
OMIM: 300366, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green TLR8 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.114

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Immunodeficiency 98 with autoinflammation, X-linked, MIM# 301078
    Tags
    • somatic

    Green TLR8 in Mendeliome


    Version 1.2374

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Immunodeficiency 98 with autoinflammation, X-linked, MIM# 301078
    Tags
    • somatic

    Green TLR8 in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 1.115

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Immunodeficiency 98 with autoinflammation, X-linked, MIM# 301078
    Tags
    • somatic

    Green TLR8 in Defects of intrinsic and innate immunity


    Level 2: Immunological disorders
    Version 1.20

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Immunodeficiency 98 with autoinflammation, X-linked, MIM# 301078

    Green TLR8 in Autoinflammatory Disorders


    Level 2: Immunological disorders
    Version 2.3

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Autoinflammatory syndrome MONDO:0019751, TLR8-associated