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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Mink1 and congenital myasthenic syndrome in Heterocephalus glaber.        

  • 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 MINK1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 183 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 0 papers in RGD have been used to annotate Mink1
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive | ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:10496269 PMID:10514102 PMID:10534268 PMID:15322984 PMID:15367858 PMID:17363247 PMID:25326635 PMID:25741868 PMID:26467025 PMID:27634344 PMID:28492532 PMID:9097970 PMID:9668239


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