Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 GeneticVariation disease BEFREE A mutation in FoxN1 generates alymphoid cystic thymic dysgenesis due to defective TECs, causing primary T-cell immunodeficiency, named Nude/SCID syndrome, and leads to a hairless "nude" phenotype in both mice and humans. 24432845 2014
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease 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 		0.910 Biomarker disease 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 		0.910 GeneticVariation disease CLINVAR Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population. 15180707 2004
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease GENOMICS_ENGLAND Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation. 11159512 2001
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease 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 		0.910 GermlineCausalMutation disease ORPHANET Exposing the human nude phenotype. 10206641 1999
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 GeneticVariation disease CLINVAR Exposing the human nude phenotype. 10206641 1999
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease GENOMICS_ENGLAND Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs. 8911612 1996
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease MGD Two genetically separable steps in the differentiation of thymic epithelium. 8629026 1996
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease MGD Thymus dysgenesis in nude (nu nu) mice. 5493276 1970
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127 1969
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease MGD Absence of thymus in a mouse mutant. 5639157 1968
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease MGD 'Nude', a new hairless gene with pleiotropic effects in the mouse. 5980117 1966
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease CTD_human
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 8456
Gene Symbol: FOXN1
FOXN1 		0.910 CausalMutation disease CLINVAR