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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Foxn1 and T-cell immunodeficiency, congenital alopecia, and nail dystrophy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with FOXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to T-cell immunodeficiency, congenital alopecia, and nail dystrophy  (DOID:0060769)
  • 9 papers in RGD have been used to annotate Foxn1


    • An association has been curated linking Foxn1 and T-cell immunodeficiency, congenital alopecia, and nail dystrophy in Mus musculus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 1 RGD objects have been annotated to T-cell immunodeficiency, congenital alopecia, and nail dystrophy  (DOID:0060769)
  • 9 papers in RGD have been used to annotate Foxn1
  • Curation Notes: OMIM:601705


    • An association has been curated linking Foxn1 and T-cell immunodeficiency, congenital alopecia, and nail dystrophy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FOXN1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to T-cell immunodeficiency, congenital alopecia, and nail dystrophy  (DOID:0060769)
  • 9 papers in RGD have been used to annotate Foxn1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Foxn1 and T-cell immunodeficiency, congenital alopecia, and nail dystrophy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FOXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to T-cell immunodeficiency, congenital alopecia, and nail dystrophy  (DOID:0060769)
  • 9 papers in RGD have been used to annotate Foxn1
  • Curation Notes: ClinVar Annotator: match by term: T-cell immunodeficiency, congenital alopecia, and nail dystrophy
  • Original References(s): PMID:10206641 PMID:15180707 PMID:15897400 PMID:16199547 PMID:17576681 PMID:18339010 PMID:20864124 PMID:20978268 PMID:21507891 PMID:24033266 PMID:25173801 PMID:25741868 PMID:27484032 PMID:28492532 PMID:28636882 PMID:31447097 PMID:31566583 PMID:33464451 PMID:37419334 PMID:8911612 PMID:9536098


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