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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Prph2 and cone-rod dystrophy in Mus musculus.        

  • 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 PRPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 122 RGD objects have been annotated to cone-rod dystrophy  (DOID:0050572)
  • 39 papers in RGD have been used to annotate Prph2
  • Curation Notes: ClinVar Annotator: match by term: Cone-Rod Dystrophy, Dominant | ClinVar Annotator: match by term: Cone-Rod Dystrophy, Recessive | ClinVar Annotator: match by term: Cone-rod degeneration | ClinVar Annotator: match by term: Cone-rod dystrophy
  • Original References(s): PMID:10193525 PMID:10532447 PMID:11139241 PMID:11704030 PMID:14510799 PMID:14557183 PMID:15370544 PMID:15779916 PMID:16019073 PMID:16113362 PMID:16767206 PMID:16799052 PMID:16885924 PMID:16916875 PMID:17504850 PMID:17576681 PMID:17653047 PMID:17698758 PMID:18310263 PMID:19038374 PMID:19262438 PMID:20213611 PMID:20640437 PMID:21071739 PMID:22183351 PMID:22466463 PMID:22863181 PMID:23950152 PMID:24463884 PMID:24608669 PMID:24629188 PMID:25001182 PMID:25082885 PMID:25097241 PMID:25268133 PMID:25474345 PMID:25675413 PMID:25741868 PMID:25803555 PMID:26061163 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26667666 PMID:26796962 PMID:26842753 PMID:27365499 PMID:27884173 PMID:28492530 PMID:28492532 PMID:28559085 PMID:28838317 PMID:29343940 PMID:29555955 PMID:30718709 PMID:30726412 PMID:30926958 PMID:31213501 PMID:31429209 PMID:31456290 PMID:31574917 PMID:32531846 PMID:32717343 PMID:33546218 PMID:34906470 PMID:7493155 PMID:8015786 PMID:8111389 PMID:8302543 PMID:8485575 PMID:8485576 PMID:8675410 PMID:8747448 PMID:8994365 PMID:9010868 PMID:9279751 PMID:9331261 PMID:9443872 PMID:9536098


    • An association has been curated linking Prph2 and cone-rod dystrophy in Mus musculus.        

  • 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 PRPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 122 RGD objects have been annotated to cone-rod dystrophy  (DOID:0050572)
  • 39 papers in RGD have been used to annotate Prph2
  • Curation Notes: ClinVar Annotator: match by term: Cone-Rod Dystrophy, Dominant | ClinVar Annotator: match by term: Cone-Rod Dystrophy, Recessive | ClinVar Annotator: match by term: Cone-rod degeneration | ClinVar Annotator: match by term: Cone-rod dystrophy
  • Original References(s): PMID:10193525 PMID:10532447 PMID:11139241 PMID:11704030 PMID:14510799 PMID:14557183 PMID:15370544 PMID:15779916 PMID:16019073 PMID:16113362 PMID:16799052 PMID:16885924 PMID:17576681 PMID:17653047 PMID:17698758 PMID:18310263 PMID:19038374 PMID:19262438 PMID:20213611 PMID:20640437 PMID:21071739 PMID:22183351 PMID:22466463 PMID:22863181 PMID:23950152 PMID:24463884 PMID:24608669 PMID:24629188 PMID:25001182 PMID:25082885 PMID:25097241 PMID:25268133 PMID:25474345 PMID:25675413 PMID:25741868 PMID:25803555 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26667666 PMID:26842753 PMID:27884173 PMID:28492530 PMID:28492532 PMID:28559085 PMID:28838317 PMID:29343940 PMID:29555955 PMID:30718709 PMID:30726412 PMID:30926958 PMID:31213501 PMID:31429209 PMID:31456290 PMID:31574917 PMID:32531846 PMID:32717343 PMID:33546218 PMID:7493155 PMID:8015786 PMID:8302543 PMID:8485576 PMID:8675410 PMID:8747448 PMID:8994365 PMID:9010868 PMID:9279751 PMID:9331261 PMID:9443872 PMID:9536098


    • An association has been curated linking Prph2 and cone-rod dystrophy in Mus musculus.        

  • 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 PRPH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 122 RGD objects have been annotated to cone-rod dystrophy  (DOID:0050572)
  • 39 papers in RGD have been used to annotate Prph2
  • Curation Notes: ClinVar Annotator: match by term: Cone-Rod Dystrophy, Dominant | ClinVar Annotator: match by term: Cone-rod degeneration | ClinVar Annotator: match by term: Cone-rod dystrophy
  • Original References(s): PMID:10193525 PMID:10532447 PMID:11139241 PMID:11704030 PMID:14510799 PMID:14557183 PMID:15370544 PMID:15779916 PMID:16019073 PMID:16113362 PMID:16767206 PMID:16799052 PMID:16885924 PMID:16916875 PMID:17504850 PMID:17576681 PMID:17653047 PMID:17698758 PMID:18310263 PMID:19038374 PMID:19262438 PMID:20213611 PMID:20640437 PMID:21071739 PMID:22183351 PMID:22466463 PMID:22863181 PMID:23950152 PMID:24463884 PMID:24608669 PMID:24629188 PMID:25001182 PMID:25082885 PMID:25097241 PMID:25268133 PMID:25474345 PMID:25675413 PMID:25741868 PMID:25803555 PMID:26061163 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26667666 PMID:26796962 PMID:26842753 PMID:27365499 PMID:27884173 PMID:28492530 PMID:28492532 PMID:28559085 PMID:28838317 PMID:29343940 PMID:29555955 PMID:30718709 PMID:30726412 PMID:30926958 PMID:31213501 PMID:31429209 PMID:31456290 PMID:31574917 PMID:32531846 PMID:32717343 PMID:33546218 PMID:34240658 PMID:34906470 PMID:7493155 PMID:8015786 PMID:8111389 PMID:8302543 PMID:8485575 PMID:8485576 PMID:8675410 PMID:8747448 PMID:8994365 PMID:9010868 PMID:9279751 PMID:9331261 PMID:9443872 PMID:9536098


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