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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Megf10 and congenital myopathy 10B in Rattus norvegicus.        

  • 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 MEGF10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital myopathy 10B  (DOID:0081345)
  • 5 papers in RGD have been used to annotate Megf10


    • An association has been curated linking Megf10 and congenital myopathy 10B in Rattus norvegicus.        

  • 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 MEGF10 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital myopathy 10B  (DOID:0081345)
  • 5 papers in RGD have been used to annotate Megf10
  • Curation Notes: ClinVar Annotator: match by term: Congenital myopathy 10b, mild variant
  • Original References(s): PMID:22101682 PMID:22371254 PMID:23954233 PMID:25741868 PMID:27460346 PMID:28492532 PMID:28498977 PMID:29128256 PMID:36349186 PMID:38703036


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