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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking GRIP1 and Fraser syndrome 1 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:11544804|RGD:11545180|RGD:11547186|RGD:11548776|RGD:11550778 (Homo sapiens) & RGD:11544804|RGD:11545180|RGD:11547186|RGD:11548776|RGD:11550778 (Homo sapiens) & RGD:11544804|RGD:11545180|RGD:11547186|RGD:11548776|RGD:11550778 (Homo sapiens) & RGD:11544804|RGD:11545180|RGD:11547186|RGD:11548776|RGD:11550778 (Homo sapiens) & RGD:11544804|RGD:11545180|RGD:11547186|RGD:11548776|RGD:11550778 (Homo sapiens)
  • 6 RGD objects have been annotated to Fraser syndrome 1  (DOID:0111405)
  • 6 papers in RGD have been used to annotate GRIP1
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 1
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking GRIP1 and Fraser syndrome 1 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:10047735|RGD:11661878 (Homo sapiens) & RGD:10047735|RGD:11661878 (Homo sapiens)
  • 6 RGD objects have been annotated to Fraser syndrome 1  (DOID:0111405)
  • 6 papers in RGD have been used to annotate GRIP1
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 1
  • Original References(s): PMID:28492532


    • An association has been curated linking GRIP1 and Fraser syndrome 1 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:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens) & RGD:11617799|RGD:11622943|RGD:11623526|RGD:11634806|RGD:11634876|RGD:11635368|RGD:11635484|RGD:11635596|RGD:11635660|RGD:11635794|RGD:11635847|RGD:11648114|RGD:11650334|RGD:11654684|RGD:11656531|RGD:11658493|RGD:11662917|RGD:156056409 (Homo sapiens)
  • 6 RGD objects have been annotated to Fraser syndrome 1  (DOID:0111405)
  • 6 papers in RGD have been used to annotate GRIP1
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 1


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