PanelApp (staging)
  1. Genes and Genomic Entities
  2. TNFAIP3

TNFAIP3

TNF alpha induced protein 3
OMIM: 191163, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green TNFAIP3 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.122

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Inflammatory bowel disease
    • Crohn's disease
    • Autoinflammatory syndrome, familial, Behcet-like

    Green TNFAIP3 in Mendeliome


    Version 1.2302

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744
    • Inflammatory bowel disease

    Green TNFAIP3 in Autoinflammatory Disorders


    Level 2: Immunological disorders
    Version 2.3

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744

    Red TNFAIP3 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.116

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Autoinflammatory syndrome, familial, Behcet-like 1 MIM#616744
    Tags
    • treatable
    • immunological