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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking OPTN and amyotrophic lateral sclerosis type 12 in Pan paniscus.        

  • 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 OPTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to amyotrophic lateral sclerosis type 12  (DOID:0060203)
  • 0 papers in RGD have been used to annotate OPTN
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 12
  • Original References(s): PMID:11834836 PMID:11978762 PMID:12208142 PMID:12789137 PMID:12939304 PMID:14597044 PMID:15226658 PMID:15312511 PMID:15326130 PMID:15370540 PMID:15547491 PMID:15557444 PMID:15761120 PMID:16148883 PMID:16199547 PMID:16205626 PMID:16358725 PMID:16619239 PMID:16885925 PMID:17122126 PMID:17293779 PMID:17359525 PMID:17389490 PMID:17615537 PMID:19096531 PMID:19145250 PMID:19172505 PMID:19672125 PMID:20428114 PMID:20671613 PMID:20981092 PMID:21074290 PMID:21217154 PMID:21220178 PMID:21550138 PMID:21613650 PMID:21852022 PMID:22402017 PMID:22708870 PMID:22722621 PMID:22892313 PMID:22995991 PMID:23062601 PMID:24683533 PMID:25333069 PMID:25681989 PMID:25741868 PMID:25741905 PMID:25943890 PMID:26467025 PMID:26503823 PMID:26566915 PMID:26740678 PMID:27485216 PMID:28492532 PMID:29411640 PMID:29525178 PMID:29650794 PMID:30519240 PMID:30739198 PMID:31108397 PMID:31198474 PMID:31838784 PMID:32028661 PMID:32579787 PMID:32893042 PMID:35896380


    • An association has been curated linking OPTN and amyotrophic lateral sclerosis type 12 in Pan paniscus.        

  • 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 OPTN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to amyotrophic lateral sclerosis type 12  (DOID:0060203)
  • 0 papers in RGD have been used to annotate OPTN


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