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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Cabp4 and Congenital Stationary Night Blindness 2B 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 CABP4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Congenital Stationary Night Blindness 2B  (DOID:9004066)
  • 7 papers in CRRD have been used to annotate Cabp4
  • Curation Notes: ClinVar Annotator: match by OMIM:610427
  • Original References(s): PMID:20157620, PMID:23099293

  • This annotation was curated on 2019-10-08 13:07:55.0 by CRRD . For more information contact us

    An association has been curated linking Cabp4 and Congenital Stationary Night Blindness 2B 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 CABP4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Congenital Stationary Night Blindness 2B  (DOID:9004066)
  • 7 papers in CRRD have been used to annotate Cabp4

  • This annotation was curated on 2019-10-09 19:57:05.0 by CRRD . For more information contact us

    An association has been curated linking Cabp4 and Congenital Stationary Night Blindness 2B 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 CABP4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Congenital Stationary Night Blindness 2B  (DOID:9004066)
  • 7 papers in CRRD have been used to annotate Cabp4
  • Curation Notes: ClinVar Annotator: match by OMIM:610427
  • Original References(s): PMID:16960802

  • This annotation was curated on 2019-10-08 13:08:54.0 by CRRD . For more information contact us

    An association has been curated linking Cabp4 and Congenital Stationary Night Blindness 2B 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 CABP4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Congenital Stationary Night Blindness 2B  (DOID:9004066)
  • 7 papers in CRRD have been used to annotate Cabp4
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 2B

  • This annotation was curated on 2019-10-08 13:06:50.0 by CRRD . For more information contact us

    An association has been curated linking Cabp4 and Congenital Stationary Night Blindness 2B 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 CABP4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Congenital Stationary Night Blindness 2B  (DOID:9004066)
  • 7 papers in CRRD have been used to annotate Cabp4
  • Curation Notes: ClinVar Annotator: match by term: Congenital stationary night blindness, type 2B
  • Original References(s): PMID:19074807, PMID:23714322, PMID:30718709

  • This annotation was curated on 2019-10-08 13:07:55.0 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.