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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Scn1b and Brugada syndrome 5 in Rattus norvegicus.        

  • 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to Brugada syndrome 5  (DOID:0110222)
  • 21 papers in RGD have been used to annotate Scn1b


    • An association has been curated linking Scn1b and Brugada syndrome 5 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 SCN1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to Brugada syndrome 5  (DOID:0110222)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: ClinVar Annotator: match by term: Brugada syndrome 5
  • Original References(s): PMID:11254444 PMID:11263970 PMID:11866477 PMID:12011299 PMID:12486163 PMID:14504340 PMID:14690046 PMID:15671291 PMID:15710580 PMID:15857929 PMID:16199547 PMID:16205844 PMID:17020904 PMID:17576681 PMID:17604911 PMID:17629415 PMID:17928445 PMID:18464934 PMID:18941776 PMID:19522081 PMID:19710327 PMID:19808477 PMID:20226894 PMID:20437590 PMID:20628201 PMID:20662403 PMID:21040232 PMID:21703448 PMID:21994374 PMID:22155597 PMID:22155598 PMID:22247482 PMID:22284586 PMID:22292491 PMID:22425777 PMID:22840528 PMID:22987075 PMID:23182416 PMID:23414114 PMID:23465283 PMID:23527921 PMID:23584539 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24065921 PMID:24529773 PMID:24567321 PMID:24605816 PMID:24623842 PMID:24662403 PMID:24747835 PMID:24848745 PMID:24981977 PMID:25253298 PMID:25421039 PMID:25668026 PMID:25741868 PMID:25827112 PMID:25998140 PMID:26042039 PMID:26129877 PMID:26467025 PMID:26498160 PMID:26704558 PMID:27207958 PMID:27216889 PMID:27277800 PMID:27435932 PMID:27707468 PMID:27896052 PMID:28074886 PMID:28218389 PMID:28331474 PMID:28341588 PMID:28449774 PMID:28488083 PMID:28492532 PMID:28600387 PMID:28681755 PMID:28717674 PMID:28726809 PMID:28837624 PMID:29056246 PMID:29358611 PMID:29572929 PMID:29655203 PMID:29758173 PMID:29915715 PMID:29924869 PMID:29992740 PMID:30182498 PMID:30660056 PMID:31069529 PMID:31465153 PMID:31709768 PMID:31729702 PMID:31737628 PMID:31980526 PMID:32192759 PMID:32369273 PMID:32466254 PMID:32593896 PMID:32613771 PMID:32651551 PMID:32931854 PMID:33552729 PMID:33901312 PMID:34034907 PMID:36011376 PMID:36288729 PMID:36413997 PMID:37845033 PMID:9461582 PMID:9536098 PMID:9539778 PMID:9697698 PMID:9894880


    • An association has been curated linking Scn1b and Brugada syndrome 5 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 SCN1B (Homo sapiens) [(EXP) inferred from experiment]
  • 54 RGD objects have been annotated to Brugada syndrome 5  (DOID:0110222)
  • 21 papers in RGD have been used to annotate Scn1b
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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