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GENE - TERM ANNOTATION REPORT

41 Annotations Found.

An association has been curated linking Myh9 and MYH-9 related disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Seri M, etal., Hum Genet. 2002 Feb;110(2):182-6. Epub 2001 Dec 14.
  • The annotation has been inferred from sequence orthology with MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Seri M, etal., Hum Genet. 2002 Feb;110(2):182-6. Epub 2001 Dec 14.
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: DNA:missense mutation:exon:p.R702H(human)


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:25741868 PMID:31064749


  • An association has been curated linking Myh9 and MYH-9 related disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Arrondel C, etal., J Am Soc Nephrol. 2002 Jan;13(1):65-74.
  • The annotation has been inferred from sequence orthology with MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Arrondel C, etal., J Am Soc Nephrol. 2002 Jan;13(1):65-74.
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: DNA:missense mutations:exons:multiple


  • An association has been curated linking Myh9 and MYH-9 related disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Suzuki N, etal., PLoS One. 2013 Aug 20;8(8):e71187. doi: 10.1371/journal.pone.0071187. eCollection 2013.
  • The annotation has been inferred from sequence orthology with Myh9 (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Suzuki N, etal., PLoS One. 2013 Aug 20;8(8):e71187. doi: 10.1371/journal.pone.0071187. eCollection 2013.
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: DNA:mutation:cds:p.R702C(mouse)


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by OMIM:155100
  • Original References(s): PMID:15667538


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:12621333


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9 related disorders
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking Myh9 and MYH-9 related disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Yi Y, etal., Clin Chim Acta. 2006 Nov;373(1-2):49-54. Epub 2006 May 16.
  • The annotation has been inferred from sequence orthology with MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype, (IEP) inferred from expression pattern]
  • 3 additional annotations were made from Yi Y, etal., Clin Chim Acta. 2006 Nov;373(1-2):49-54. Epub 2006 May 16.
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: DNA:mutation:exon:p.E1841K(human)


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by OMIM:155100
  • Original References(s): PMID:12792306 PMID:19450438


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by OMIM:153640
  • Original References(s): PMID:10973259 PMID:11093280


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by OMIM:155100
  • Original References(s): PMID:10973260 PMID:12792306


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Epstein syndrome
  • Original References(s): PMID:24033266 PMID:24875298 PMID:25741868


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:10973259 PMID:11590545 PMID:12621333


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:25741868


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9 related disorders
  • Original References(s): PMID:11159552 PMID:11590545 PMID:12621333 PMID:12649151 PMID:12792306 PMID:1449176 PMID:25741868


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Sebastian syndrome
  • Original References(s): PMID:15613099


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Sebastian syndrome
  • Original References(s): PMID:11023810 PMID:17146397 PMID:24890873 PMID:25505834 PMID:9390828


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:19557653 PMID:23144074 PMID:24033266 PMID:26346198 PMID:26969326 PMID:27068579 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:18059020 PMID:24033266


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:24130771 PMID:25077172 PMID:26467025 PMID:28492532 PMID:30720677


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Sebastian syndrome
  • Original References(s): PMID:10973259 PMID:25741868


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Epstein syndrome
  • Original References(s): PMID:11752022 PMID:12533692 PMID:16969870 PMID:23409987 PMID:24186861 PMID:25741868 PMID:26226608


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Sebastian syndrome
  • Original References(s): PMID:10739770 PMID:10973259 PMID:10973260 PMID:11590545 PMID:25741868 PMID:29090586


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: May-Hegglin anomaly
  • Original References(s): PMID:10973259 PMID:10973260 PMID:11590545 PMID:25741868 PMID:8280620


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Sebastian syndrome
  • Original References(s): PMID:10603121 PMID:10973259 PMID:11590545 PMID:12792306 PMID:25741868 PMID:5011389


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
  • Original References(s): PMID:11752022 PMID:18676005 PMID:22123909 PMID:22477015 PMID:22995991 PMID:24033266 PMID:24643058 PMID:25741868 PMID:26467025 PMID:28059092 PMID:29090586 PMID:30720677


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:23349334 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:24033266 PMID:25752595


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
  • Original References(s): PMID:11590545 PMID:20588287 PMID:23804846 PMID:24033266 PMID:24643058 PMID:25077172 PMID:25949529


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: MYH9-related disorder
  • Original References(s): PMID:23144074


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
  • Original References(s): PMID:11590545 PMID:11935325 PMID:25741868 PMID:31064749


  • An association has been curated linking Myh9 and MYH-9 related disease 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYH-9 related disease  (DOID:0060651)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27610647


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