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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Fktn and Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4 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 FKTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4  (DOID:9005845)
  • 19 papers in RGD have been used to annotate Fktn


  • An association has been curated linking Fktn and Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4 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 FKTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4  (DOID:9005845)
  • 19 papers in RGD have been used to annotate Fktn
  • Curation Notes: ClinVar Annotator: match by OMIM:613152
  • Original References(s): PMID:19299310


  • An association has been curated linking Fktn and Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4 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 FKTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4  (DOID:9005845)
  • 19 papers in RGD have been used to annotate Fktn
  • Curation Notes: ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, FKTN-RELATED
  • Original References(s): PMID:19015585 PMID:23582336 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Fktn and Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4 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 FKTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Muscular Dystrophy-Dystroglycanopathy (congenital without mental retardation), Type B, 4  (DOID:9005845)
  • 19 papers in RGD have been used to annotate Fktn
  • Curation Notes: ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, FKTN-RELATED
  • Original References(s): PMID:17044012 PMID:17878207 PMID:19179078 PMID:19299310 PMID:19396839 PMID:20961758 PMID:25821721 PMID:26923585 PMID:28492532 PMID:30060766


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