TNFRSF13B - Gene browser

TNFRSF13B

TNF receptor superfamily member 13B

HCNC Approved Symbol: TNFRSF13B (HGNC:18153)
Genomic Coordinates: 17:16,939,081 - 16,972,118 (17p11.2)
Synonyms: TACI, CD267, IGAD2
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

26Patients

In total, 26 patients were diagnosed with a variant in the TNFRSF13B gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

026
Patient count

Autoimmunity: 7 (26.9%)
Patient Count: 7 (26.9%)
% of total patients presenting each phenotype is shown in parentheses.
7 (26.9%)
Humoral immunodeficiency: 7 (26.9%)
Patient Count: 7 (26.9%)
% of total patients presenting each phenotype is shown in parentheses.
7 (26.9%)
Recurrent infections: 6 (23.1%)
Patient Count: 6 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
6 (23.1%)
Immunodeficiency: 4 (15.4%)
Patient Count: 4 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (15.4%)
Neutropenia: 3 (11.5%)
Patient Count: 3 (11.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (11.5%)