TNFRSF13B

TNF receptor superfamily member 13B
OMIM: 604907, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green TNFRSF13B in COVID-19 research Level 2: Viral research Version 1.146	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green IUIS Classification February 2018 A- or hypo-gammaglobulinaemia v1.25 GOSH PID v.8.0 GRID V2.0 IUIS Classification December 2019 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 GOSH PID v.8.0 A- or hypo-gammaglobulinaemia v1.25 Phenotypes IgA with IgG subclass deficiency Immunodeficiency, common variable, 2 Immunodeficiency, common variable, 2, 240500 Variable clinical expression Isolated IgG subclass deficiency IGAD Selective IgA deficiency Common variable immunodeficiency disorders (CVID) Predominantly Antibody Deficiencies Immunoglobulin A deficiency 2, 609529 CVID
Red TNFRSF13B in Primary immunodeficiency or monogenic inflammatory bowel disease Level 2: Immunology Version 8.78 Latest signed off version: v8.0 (30 Apr 2025)	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources IUIS Classification December 2019 Expert Review Red IUIS Classification February 2018 Victorian Clinical Genetics Services ESID Registry 20171117 GRID V2.0 GOSH PID v.8.0 A- or hypo-gammaglobulinaemia v1.25 Phenotypes Immunodeficiency, common variable, 2, 240500 Variable clinical expression Common variable immunodeficiency disorders (CVID) Immunodeficiency, common variable, 2 IgA with IgG subclass deficiency IGAD Isolated IgG subclass deficiency Selective IgA deficiency Immunoglobulin A deficiency 2, 609529 Predominantly Antibody Deficiencies CVID
Red TNFRSF13B in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red NHS GMS PAGE DD-Gene2Phenotype Phenotypes Immunodeficiency, common variable, 2, OMIM:240500
Green TNFRSF13B in DDG2P Version 6.424 Latest signed off version: v6.0 (30 Apr 2025) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green DD-Gene2Phenotype Phenotypes IMMUNODEFICIENCY, COMMON VARIABLE, 2 240500