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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Fhl1 and X-Linked Scapuloperoneal Muscular Dystrophy in Ictidomys tridecemlineatus.        

  • 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 FHL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-Linked Scapuloperoneal Muscular Dystrophy  (DOID:9001526)
  • 0 papers in RGD have been used to annotate Fhl1


    • An association has been curated linking Fhl1 and X-Linked Scapuloperoneal Muscular Dystrophy in Ictidomys tridecemlineatus.        

  • 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 FHL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-Linked Scapuloperoneal Muscular Dystrophy  (DOID:9001526)
  • 0 papers in RGD have been used to annotate Fhl1
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy, X-linked dominant | ClinVar Annotator: match by term: X-linked scapuloperoneal muscular dystrophy
  • Original References(s): PMID:18179888 PMID:18179901 PMID:19181672 PMID:21629301 PMID:25274776 PMID:25741868 PMID:26467025 PMID:26752647 PMID:28492532 PMID:30260394


    • An association has been curated linking Fhl1 and X-Linked Scapuloperoneal Muscular Dystrophy in Ictidomys tridecemlineatus.        

  • 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 FHL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to X-Linked Scapuloperoneal Muscular Dystrophy  (DOID:9001526)
  • 0 papers in RGD have been used to annotate Fhl1
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy, X-linked dominant | ClinVar Annotator: match by term: X-linked scapuloperoneal muscular dystrophy
  • Original References(s): PMID:18179888 PMID:18179901 PMID:19181672 PMID:19716112 PMID:21629301 PMID:24634512 PMID:25274776 PMID:25741868 PMID:26467025 PMID:26752647 PMID:28492532 PMID:30260394


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