CD79Abase: Igα deficiency

Version 1.0 last updated 14 June, 2007 contains 2 public entries


Curated:	Mauno Vihinen
Maintained by:	Jouni Väliaho
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Short description of the CD79Abase :

Igα deficiency is an autosomal recessive disorder caused by mutation in the Igα (CD79α) leading to B cell defect. Mutations in the gene for Igα as well as in other pre-B cell receptor complex as λ 5/14.1 (IGLL1) and in the the gene for μ heavy chain (IGHM), can cause a disorder clinically similar to XLA.

Other IBT bioinformatics services:
Immunodeficiency Resource (IDR)
Immunodeficiency Mutation Databases (MUTbase)
IDdiagnostics
Immunome Knowledge Base (IKB) - An integrated service for immunome research
SH2base - Database for pathogenic SH2 domain mutations

IDbases are linked to University of California Santa Cruz (UCSC) genome browser: CD79Abase