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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract 9, autosomal recessive
  • Original References(s): PMID:11006246


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by OMIM:604219
  • Original References(s): PMID:23255486


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by OMIM:604219
  • Original References(s): PMID:16862070


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by OMIM:604219
  • Original References(s): PMID:14512969, PMID:26542570


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant, multiple types, with microcornea
  • Original References(s): PMID:17724170, PMID:26694549


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:10684623, PMID:11123904, PMID:12601044, PMID:16735993, PMID:17296897, PMID:18085469, PMID:18302245, PMID:20079887, PMID:22045060, PMID:22140512, PMID:22216983, PMID:22347476, PMID:28492532, PMID:9467006


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:28492532


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:17937925, PMID:18587492, PMID:22045060, PMID:22140512, PMID:22347476, PMID:23379525, PMID:25018622, PMID:25694240, PMID:28179137, PMID:28492532


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant, multiple types, with microcornea
  • Original References(s): PMID:10684623, PMID:11123904, PMID:16564818, PMID:16735993, PMID:17296897, PMID:17724170, PMID:18085469, PMID:18302245, PMID:20079887, PMID:22045060, PMID:22140512, PMID:22216983, PMID:28492532, PMID:9467006


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:27307692


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:19182255, PMID:21042563


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant
  • Original References(s): PMID:25741868


  • An association has been curated linking Cryaa and cataract 9 multiple types 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 CRYAA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to cataract 9 multiple types  (DOID:0110266)
  • 24 papers in RGD have been used to annotate Cryaa
  • Curation Notes: ClinVar Annotator: match by term: Cataract, autosomal dominant, multiple types, with microcornea
  • Original References(s): PMID:17724170, PMID:19503744, PMID:22045060, PMID:22140512, PMID:22347476, PMID:23508780, PMID:25741868, PMID:28492532


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