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agammaglobulinemia 8A

Summary
Definition
An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.
Super Class
agammaglobulinemia autosomal dominant disease
Disease Ontology
DOID:0081140
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6929 TCF3 transcription factor 3
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P15923 Transcription factor E2-alpha
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: April 7, 2025