Immunoglobulin A Deficiency 2; Igad2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Immunoglobulin A Deficiency 2; Igad2

TNFRSF13B

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Immunoglobulin A Deficiency 2; Igad2

Immunodeficiency
Autoimmunity
IgA deficiency
Recurrent sinopulmonary infections
Recurrent infection of the gastrointestinal tract
Abnormal lymphocyte morphology

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Immunoglobulin A Deficiency 2; Igad2 Is also known as immunoglobulin a, selective deficiency of, taci-related, iga, selective deficiency of, taci-related.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Immunoglobulin A Deficiency 2; Igad2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Common Variable Immunodeficiency Syndrome (CVID): TNFRSF13B (TACI) (Full Gene Sequencing). By Molecular Diagnostic Laboratory University of Alberta (Canada). TNFRSF13B Specificity 100 % Genes 100 %
Common Variable Immunodeficiency Syndrome (CVID): TNFRSF13B (TACI) (Known Mutation). By Molecular Diagnostic Laboratory University of Alberta (Canada). TNFRSF13B Specificity 100 % Genes 100 %
TNFRSF13B Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). TNFRSF13B Specificity 100 % Genes 100 %
TNFRSF13B Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). TNFRSF13B Specificity 100 % Genes 100 %
Tier 2: Hereditary Lymphoma and Immunodeficiency Panel. By Genetic Services Laboratory University of Chicago (United States). BLM, SH2D1A, BRCA1, BRCA2, STXBP2, FAS, CD27, FASLG, WAS, IKZF1, CASP10, CARD11, TNFRSF13B, ADA, DOCK8, CTLA4, MAGT1, ITK, NBN, NF1 , (...) View the complete list with 3 more genes Panel complete gene list BLM, SH2D1A, BRCA1, BRCA2, STXBP2, FAS, CD27, FASLG, WAS, IKZF1, CASP10, CARD11, TNFRSF13B, ADA, DOCK8, CTLA4, MAGT1, ITK, NBN, NF1, ATM, PIK3CD, PRF1 Specificity 5 % Genes 100 %
Primary Antibody Deficiency Panel, Sequencing and Deletion/Duplication. By ARUP Laboratories, Molecular Genetics and Genomics (United States). SH2D1A, BTK, CD40, CD40LG, UNG, VAV1, AICDA, BLNK, CD19, CD79A, CD79B, CD81, LRBA, TNFRSF13C, TNFRSF13B, ADA, LRRC8A, CR2, ICOS, IGHM , (...) View the complete list with 15 more genes Panel complete gene list SH2D1A, BTK, CD40, CD40LG, UNG, VAV1, AICDA, BLNK, CD19, CD79A, CD79B, CD81, LRBA, TNFRSF13C, TNFRSF13B, ADA, LRRC8A, CR2, ICOS, IGHM, IGLL1, XIAP, IKBKG, MRE11, MS4A1, NBN, NFKB2, NFKBIA, ATM, PIK3CD, PIK3R1, PLCG2, PRKCD, PTPRC, RAG2 Specificity 3 % Genes 100 %
TACI-Associated Common Variable Immunodeficiency (TNFRSF13B) Sequencing. By ARUP Laboratories, Molecular Genetics and Genomics (United States). TNFRSF13B Specificity 100 % Genes 100 %
Immunoglobulin A deficiency (sequence analysis of TNFRSF13B gene). By CGC Genetics (Portugal). TNFRSF13B Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Search Engine

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