Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD Foxn1 regulates lineage progression in cortical and medullary thymic epithelial cells but is dispensable for medullary sublineage divergence. 22072979

2011
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD T cell deficiency leads to cognitive dysfunction: implications for therapeutic vaccination for schizophrenia and other psychiatric conditions. 15141078

2004
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD Forkhead/winged-helix transcription factor Whn regulates hair keratin gene expression: molecular analysis of the nude skin phenotype. 10767081

2000
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD Two genetically separable steps in the differentiation of thymic epithelium. 8629026

1996
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD Thymus dysgenesis in nude (nu nu) mice. 5493276

1970
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127

1969
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD Absence of thymus in a mouse mutant. 5639157

1968
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker MGD 'Nude', a new hairless gene with pleiotropic effects in the mouse. 5980117

1966
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker MGD T cell deficiency leads to cognitive dysfunction: implications for therapeutic vaccination for schizophrenia and other psychiatric conditions. 15141078

2004
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker MGD Thymus dysgenesis in nude (nu nu) mice. 5493276

1970
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127

1969
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker MGD Absence of thymus in a mouse mutant. 5639157

1968
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker MGD 'Nude', a new hairless gene with pleiotropic effects in the mouse. 5980117

1966
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD Foxn1 regulates lineage progression in cortical and medullary thymic epithelial cells but is dispensable for medullary sublineage divergence. 22072979

2011
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD T cell deficiency leads to cognitive dysfunction: implications for therapeutic vaccination for schizophrenia and other psychiatric conditions. 15141078

2004
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD Forkhead/winged-helix transcription factor Whn regulates hair keratin gene expression: molecular analysis of the nude skin phenotype. 10767081

2000
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD Two genetically separable steps in the differentiation of thymic epithelium. 8629026

1996
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD Thymus dysgenesis in nude (nu nu) mice. 5493276

1970
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127

1969
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD Absence of thymus in a mouse mutant. 5639157

1968
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker MGD 'Nude', a new hairless gene with pleiotropic effects in the mouse. 5980117

1966