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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Wright SD, etal., Blood. 1993 May 1;81(9):2339-47.
  • The annotation has been inferred from sequence orthology with GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Wright SD, etal., Blood. 1993 May 1;81(9):2339-47.
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: DNA:missense mutations:cds:p.D21G, p.N45S (human)

  • This annotation was curated on 2016-01-21 17:05:02.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:9886312

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:11167791

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:8481514

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:12100158, PMID:13442197

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:14510954, PMID:25370924, PMID:25741868, PMID:8049428, PMID:8481514

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . For more information contact us

    An association has been curated linking Gp9 and Bernard-Soulier Syndrome, Type C 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 GP9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Bernard-Soulier Syndrome, Type C  (DOID:9001316)
  • 10 papers in CRRD have been used to annotate Gp9
  • Curation Notes: ClinVar Annotator: match by term: Bernard-Soulier syndrome type C
  • Original References(s): PMID:25741868, PMID:9163595

  • This annotation was curated on 2019-11-12 07:32:26.0 by CRRD . 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.