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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking GCKR and genetic disease 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:401758228 (Homo sapiens)
  • 33189 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate GCKR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28106320


    • An association has been curated linking GCKR and genetic disease 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:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens) & RGD:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens) & RGD:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens) & RGD:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens) & RGD:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens) & RGD:151718685|RGD:155716359|RGD:156001328|RGD:156119533|RGD:156131008|RGD:401894302 (Homo sapiens)
  • 33189 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate GCKR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking GCKR and genetic disease 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:401762281 (Homo sapiens)
  • 33189 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate GCKR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28106320 PMID:28492532


    • An association has been curated linking GCKR and genetic disease 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:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens) & RGD:155905886|RGD:155922762|RGD:155931445|RGD:156009860|RGD:156016318|RGD:156115261|RGD:156187235|RGD:156222282|RGD:156225620|RGD:156231025|RGD:156317023|RGD:156348515|RGD:156362280|RGD:156396247|RGD:329388687|RGD:401722417|RGD:401731159|RGD:401743430|RGD:401758325|RGD:401759565|RGD:401769370|RGD:401890062|RGD:401890953 (Homo sapiens)
  • 33189 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate GCKR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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