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Standards Ontologies Notations
immunoglobulin alpha deficiency

Summary
Synonym
  • IgA deficiency
  • gamma-A-globulin deficiency
Definition
A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.
Super Class
B cell deficiency autosomal recessive disease
Disease Ontology
DOID:0060025
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
1493 CTLA4 cytotoxic T-lymphocyte associated protein 4
3119 HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
29851 ICOS inducible T cell costimulator
Displaying all 3 entries
Gene ID Gene Symbol Description Source
12477 Ctla4 cytotoxic T-lymphocyte-associated protein 4
14961 H2-Ab1 histocompatibility 2, class II antigen A, beta 1
54167 Icos inducible T cell co-stimulator
Displaying 1 entry
Gene ID Gene Symbol Description Source
64545 Icos inducible T-cell co-stimulator
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024