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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Mertk and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MERTK (Homo sapiens) [(EXP) inferred from experiment]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 13 papers in RGD have been used to annotate Mertk
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:11062461


    • An association has been curated linking Mertk and retinitis pigmentosa 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 MERTK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 13 papers in RGD have been used to annotate Mertk
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:11062461 PMID:11592982 PMID:15111602 PMID:16199547 PMID:16714263 PMID:17301963 PMID:17576681 PMID:19956407 PMID:20300561 PMID:22180149 PMID:22939401 PMID:24265693 PMID:24625443 PMID:24938718 PMID:25097241 PMID:25741868 PMID:26263531 PMID:26355662 PMID:26700204 PMID:27208204 PMID:28041643 PMID:28492532 PMID:28559085 PMID:29068140 PMID:29659094 PMID:30054919 PMID:30718709 PMID:31725702 PMID:9536098


    • An association has been curated linking Mertk and retinitis pigmentosa 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 MERTK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 13 papers in RGD have been used to annotate Mertk
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:11062461 PMID:15111602 PMID:16199547 PMID:16714263 PMID:17301963 PMID:17576681 PMID:19956407 PMID:20300561 PMID:22180149 PMID:22939401 PMID:24265693 PMID:24625443 PMID:24938718 PMID:25097241 PMID:25324289 PMID:25741868 PMID:25741905 PMID:25741913 PMID:25741914 PMID:26355662 PMID:26700204 PMID:27208204 PMID:28041643 PMID:28492532 PMID:28559085 PMID:29068140 PMID:29659094 PMID:30054919 PMID:30718709 PMID:31054281 PMID:31725702 PMID:32036094 PMID:33353011 PMID:34906470 PMID:36909829 PMID:9536098


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