TNFRSF13C

TNF receptor superfamily member 13C
OMIM: 606269, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green TNFRSF13C in COVID-19 research


Level 2: Viral research
Version 1.147

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • IUIS Classification February 2018
  • IUIS Classification December 2019
  • GRID V2.0
  • Victorian Clinical Genetics Services
  • ESID Registry 20171117
  • IUIS Classification December 2019
  • IUIS Classification February 2018
  • Victorian Clinical Genetics Services
  • ESID Registry 20171117
  • GRID V2.0
Phenotypes
  • Immunodeficiency, common variable, 4
  • Variable clinical expression
  • Isolated IgG subclass deficiency
  • Common variable immunodeficiency disorders (CVID)
  • Predominantly Antibody Deficiencies
Amber TNFRSF13C in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.85
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • IUIS Classification December 2019
  • Expert Review Amber
  • IUIS Classification February 2018
  • Victorian Clinical Genetics Services
  • ESID Registry 20171117
  • GRID V2.0
Phenotypes
  • Variable clinical expression
  • Common variable immunodeficiency disorders (CVID)
  • Immunodeficiency, common variable, 4
  • Isolated IgG subclass deficiency
  • Predominantly Antibody Deficiencies