Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking Cep290 and Leber congenital amaurosis in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Boye SE, etal., PLoS One. 2014 Mar 26;9(3):e92928. doi: 10.1371/journal.pone.0092928. eCollection 2014.
  • The annotation has been inferred from sequence orthology with Cep290 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Boye SE, etal., PLoS One. 2014 Mar 26;9(3):e92928. doi: 10.1371/journal.pone.0092928. eCollection 2014.
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290

  • This annotation was curated on 2018-04-21 09:00:27.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber's amaurosis
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-09-10 06:49:53.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber's amaurosis
  • Original References(s): PMID:28492532

  • This annotation was curated on 2019-09-10 06:49:53.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis

  • This annotation was curated on 2019-09-10 06:50:37.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-09-10 06:49:08.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber's amaurosis
  • Original References(s): PMID:18414213, PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-09-10 06:44:56.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:16682970, PMID:26092869, PMID:28041643

  • This annotation was curated on 2019-09-10 06:49:35.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:17564967, PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-09-10 06:48:50.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-09-10 06:50:02.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:25741868, PMID:26467025

  • This annotation was curated on 2019-09-10 06:44:55.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:17564974, PMID:19466712, PMID:19764032, PMID:26092869, PMID:28492532, PMID:30718709

  • This annotation was curated on 2019-09-10 06:47:50.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:28492532, PMID:30718709

  • This annotation was curated on 2019-09-10 06:50:13.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:30718709

  • This annotation was curated on 2019-09-10 06:48:12.0 by RGD . For more information contact us

    An association has been curated linking Cep290 and Leber congenital amaurosis 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 CEP290 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 63 RGD objects have been annotated to Leber congenital amaurosis  (DOID:14791)
  • 16 papers in RGD have been used to annotate Cep290
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis
  • Original References(s): PMID:20690115, PMID:28492532, PMID:30718709

  • This annotation was curated on 2019-09-10 06:48:02.0 by RGD . For more information contact us

    Go Back to source page   Continue to Ontology report



    NHLBI Logo

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