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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:9002651
Term: T-CELL LYMPHOPENIA, INFANTILE, WITH OR WITHOUT NAIL DYSTROPHY, AUTOSOMAL DOMINANT
Definition: An autosomal dominant disorder characterized by decreased numbers of T cells, particularly cytotoxic CD8+ T cells, usually apparent from infancy.
Definition Source(s): OMIM:618806
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 7240710OMIM  
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:25741868 PMID:28492532
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:28492532 PMID:31447097 PMID:31566583
FOXN1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:31447097
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:28492532 PMID:31447097
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:28492532 PMID:31447097 PMID:31566583 PMID:33464451
FOXN1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:25741868 PMID:28492532 PMID:31566583
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:25741868
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:10206641 PMID:15180707 PMID:25741868 PMID:28492532 PMID:31447097
FOXN1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominantPMID:10206641 PMID:15180707 PMID:15897400 PMID:18339010 PMID:20864124 PMID:20978268 PMID:21507891 PMID:28492532 PMID:28636882 PMID:31447097 PMID:8911612
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