BTK

Bruton tyrosine kinase
OMIM: 300300, Gene2Phenotype

13 panels

Panel Reviews Mode of inheritance Details
13 panels

Green BTK in Vasculitis


Level 2: Immunological disorders
Version 0.82

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Red BTK in Cataract


Level 2: Ophthalmological disorders
Version 0.366

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • X-linked agammaglobulinemia
  • isolated growth hormone deficiency type III with agammaglobulinemia

Green BTK in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.121

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green BTK in Mendeliome


    Version 1.1902

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Agammaglobulinaemia, X-linked 1, MIM# 300755
    • Isolated growth hormone deficiency, type III, with agammaglobulinaemia, MIM# 307200
    Tags
    • treatable

    Green BTK in Predominantly Antibody Deficiency


    Level 2: Immunological disorders
    Version 0.135

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Agammaglobulinaemia, X-linked 1, MIM# 300755
    • Isolated growth hormone deficiency, type III, with agammaglobulinaemia, MIM# 307200
    Tags
    • treatable

    Green BTK in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Agammaglobulinemia and isolated hormone deficiency, 307200 (3)

    Green BTK in Pituitary hormone deficiency


    Level 2: Endocrine disorders
    Version 0.34

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Isolated growth hormone deficiency, type III, with agammaglobulinemia (307200)

    Red BTK in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 0.192

    review Unknown
    Sources
    • Expert Review Red
    • NHS GMS

    Green BTK in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Agammaglobulinemia, X-linked 1

    Green BTK in Growth failure


    Version 1.76

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Isolated growth hormone deficiency, type III, with agammaglobulinaemia, MIM# 307200

    Green BTK in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Agammaglobulinemia and isolated hormone deficiency, 307200 (3)

    Green BTK in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    • BeginNGS
    Phenotypes
    • Agammaglobulinemia, X-linked 1, MIM#300755
    Tags
    • treatable
    • immunological

    Green BTK in Prepair 500+


    Level 2: Screening
    Version 1.1

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Agammaglobulinemia and isolated hormone deficiency, 307200 (3)