Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Myl2 and hypertrophic cardiomyopathy 1 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 MYL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 58 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 14 papers in RGD have been used to annotate Myl2
  • Curation Notes: ClinVar Annotator: match by term: Familial hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 19 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis
  • Original References(s): PMID:08673105 PMID:09535554 PMID:11102452 PMID:11748309 PMID:12404107 PMID:12668451 PMID:12707239 PMID:12818575 PMID:14594949 PMID:15483641 PMID:15706574 PMID:16837010 PMID:18506004 PMID:18533079 PMID:18929571 PMID:19150977 PMID:20173211 PMID:20855589 PMID:21310275 PMID:21415409 PMID:21723297 PMID:21835320 PMID:22091967 PMID:22260945 PMID:22797899 PMID:22958901 PMID:23197161 PMID:23283745 PMID:23299917 PMID:23343568 PMID:23396983 PMID:23727233 PMID:23785128 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24111713 PMID:24793961 PMID:24842367 PMID:25324513 PMID:25333069 PMID:25351510 PMID:25524337 PMID:25637381 PMID:25741868 PMID:26116789 PMID:26187847 PMID:26284228 PMID:26664906 PMID:26914223 PMID:27153395 PMID:27435932 PMID:27483260 PMID:27532257 PMID:27600940 PMID:28166811 PMID:28223422 PMID:28467684 PMID:28492532 PMID:28518168 PMID:28771489 PMID:29398688 PMID:29452157 PMID:29710196 PMID:30403391 PMID:30430732 PMID:31019283 PMID:8673105 PMID:9535554


  • An association has been curated linking Myl2 and hypertrophic cardiomyopathy 1 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 MYL2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 58 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 14 papers in RGD have been used to annotate Myl2
  • Curation Notes: ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis
  • Original References(s): PMID:08673105 PMID:09535554 PMID:11102452 PMID:11748309 PMID:12404107 PMID:12668451 PMID:12707239 PMID:12818575 PMID:14594949 PMID:15483641 PMID:15706574 PMID:16837010 PMID:18506004 PMID:18533079 PMID:18929571 PMID:19150977 PMID:20173211 PMID:20855589 PMID:21310275 PMID:21415409 PMID:21723297 PMID:21835320 PMID:22091967 PMID:22260945 PMID:22797899 PMID:22958901 PMID:23197161 PMID:23283745 PMID:23299917 PMID:23343568 PMID:23396983 PMID:23727233 PMID:23785128 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24111713 PMID:24793961 PMID:24842367 PMID:25132132 PMID:25324513 PMID:25333069 PMID:25351510 PMID:25524337 PMID:25637381 PMID:25741868 PMID:26116789 PMID:26187847 PMID:26284228 PMID:26664906 PMID:26906074 PMID:26914223 PMID:27153395 PMID:27435932 PMID:27483260 PMID:27532257 PMID:27600940 PMID:28223422 PMID:28356264 PMID:28467684 PMID:28492532 PMID:28518168 PMID:28750076 PMID:28771489 PMID:29253866 PMID:29398688 PMID:29452157 PMID:29710196 PMID:30365366 PMID:30403391 PMID:30430732 PMID:30706179 PMID:30775854 PMID:30796699 PMID:31019283 PMID:31104103 PMID:31315475 PMID:31323898 PMID:31771554 PMID:31847883 PMID:32746448 PMID:33190526 PMID:33337957 PMID:33495596 PMID:33495597 PMID:33558530 PMID:33732734 PMID:34935411 PMID:35026164 PMID:35993536 PMID:8673105 PMID:9535554


  • Go Back to source page   Continue to Ontology report