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GENE - TERM ANNOTATION REPORT

RGD ID: 1349825
Species: Homo sapiens
RGD Object: Gene
Symbol: FOXN1
Name: forkhead box N1
Acc ID: DOID:11200
Term: T cell deficiency
Definition: A primary immunodeficiency disease that is characterized by decreased numbers of circulating or functioning T cells. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/T_cell_deficiency "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/18755723 "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)
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-lymphocyte deficiencyPMID:10206641 PMID:15180707 PMID:28492532 PMID:31447097 PMID:31566583
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-lymphocyte deficiencyPMID:31566583
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