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GENE - TERM ANNOTATION REPORT

28 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)

  • This annotation was curated on 2018-05-05 09:00:33.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2018-05-05 09:01:16.0 by RGD . For more information contact us

    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)

  • This annotation was curated on 2018-05-05 09:02:12.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 04:45:42.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:16:28.0 by RGD . For more information contact us

    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)

  • This annotation was curated on 2018-05-05 09:03:28.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-06 19:57:09.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:22.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:10:55.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 04:41:30.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:16:36.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:16:36.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:15:43.0 by RGD . For more information contact us

    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:11590545, PMID:20588287, PMID:24033266, PMID:24643058, PMID:25077172

  • This annotation was curated on 2019-11-05 08:14:03.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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:11590545, PMID:11935325, PMID:25741868

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:22.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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:11752022, PMID:22123909, PMID:22477015, PMID:22995991, PMID:24033266, PMID:25741868

  • This annotation was curated on 2019-11-05 08:16:28.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:22.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:13:21.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:10:11.0 by RGD . For more information contact us

    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

  • This annotation was curated on 2019-11-05 08:16:28.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.