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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor predisposition syndrome
  • Original References(s): PMID:28492532

  • 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 Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor predisposition syndrome

  • This annotation was curated on 2019-11-05 08:16:29.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor predisposition syndrome
  • Original References(s): PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-11-05 08:15:53.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-11-05 08:16:30.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28202063, PMID:28492532

  • 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 Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-11-05 08:15:27.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:24894818, PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-11-05 08:15:26.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:24755471, PMID:24894818, PMID:25741868, PMID:26787654, PMID:28492532

  • This annotation was curated on 2019-11-05 08:14:59.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor predisposition syndrome
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-11-05 08:16:31.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:16415040, PMID:28492532, PMID:9590180

  • This annotation was curated on 2019-11-05 08:15:47.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:16415040, PMID:25741868, PMID:28492532, PMID:9590180

  • This annotation was curated on 2019-11-05 08:15:12.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:26467025, PMID:26976419, PMID:28492532

  • This annotation was curated on 2019-11-05 08:15:20.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:26467025

  • This annotation was curated on 2019-11-05 08:16:29.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:25741868, PMID:26681312, PMID:28492532, PMID:29093764

  • This annotation was curated on 2019-11-05 08:12:05.0 by RGD . For more information contact us

    An association has been curated linking Nbn and Tumor Predisposition Syndrome 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 NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 46 RGD objects have been annotated to Tumor Predisposition Syndrome  (DOID:9002089)
  • 25 papers in RGD have been used to annotate Nbn
  • Curation Notes: ClinVar Annotator: match by term: Tumor susceptibility linked to germline BAP1 mutations
  • Original References(s): PMID:16415040, PMID:25741868, PMID:26315354, PMID:28492532, PMID:9590180

  • This annotation was curated on 2019-11-05 08:14:13.0 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.