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GENE - TERM ANNOTATION REPORT

RGD ID: 1595998
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Tnfrsf13b
Name: TNF receptor superfamily member 13B
Acc ID: DOID:0060025
Term: immunoglobulin alpha 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. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Selective_immunoglobulin_A_deficiency "DO" "DO", http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112205 "DO" "DO", http://www.ncbi.nlm.nih.gov/gene/973? "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
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