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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking CEP290 and Encephalocele in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:10448705 (Homo sapiens)
  • 35 RGD objects have been annotated to Encephalocele  (DOID:9000983)
  • 19 papers in RGD have been used to annotate CEP290
  • Curation Notes: ClinVar Annotator: match by term: Occipital encephalocele
  • Original References(s): PMID:16909394 PMID:17345604 PMID:20683928 PMID:20690115 PMID:25741868 PMID:26092869 PMID:28492532 PMID:29398085


  • An association has been curated linking CEP290 and Encephalocele in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:13612371 (Homo sapiens)
  • 35 RGD objects have been annotated to Encephalocele  (DOID:9000983)
  • 19 papers in RGD have been used to annotate CEP290
  • Curation Notes: ClinVar Annotator: match by term: Occipital encephalocele
  • Original References(s): PMID:25741868


  • An association has been curated linking CEP290 and Encephalocele in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:10448757 (Homo sapiens)
  • 35 RGD objects have been annotated to Encephalocele  (DOID:9000983)
  • 19 papers in RGD have been used to annotate CEP290
  • Curation Notes: ClinVar Annotator: match by term: Occipital encephalocele
  • Original References(s): PMID:16909394 PMID:17345604 PMID:17564967 PMID:20690115 PMID:21866095 PMID:23847139 PMID:25741868 PMID:26092869 PMID:28492532 PMID:28497568 PMID:31734136


  • An association has been curated linking CEP290 and Encephalocele in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:40814211 (Homo sapiens)
  • 35 RGD objects have been annotated to Encephalocele  (DOID:9000983)
  • 19 papers in RGD have been used to annotate CEP290
  • Curation Notes: ClinVar Annotator: match by term: Encephalocele
  • Original References(s): PMID:16909394 PMID:17345604 PMID:17705300 PMID:20690115 PMID:25741868 PMID:28492532 PMID:31680349


  • An association has been curated linking CEP290 and Encephalocele in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8595382 (Homo sapiens)
  • 35 RGD objects have been annotated to Encephalocele  (DOID:9000983)
  • 19 papers in RGD have been used to annotate CEP290
  • Curation Notes: ClinVar Annotator: match by term: Encephalocele
  • Original References(s): PMID:16909394 PMID:17345604 PMID:17564974 PMID:17705300 PMID:20690115 PMID:25525159 PMID:25741868 PMID:27894351 PMID:28492532 PMID:31680349


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