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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking PRKCD 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:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens) & RGD:11525893|RGD:126922146|RGD:14705597|RGD:14732416|RGD:151821357|RGD:156174741|RGD:26899874|RGD:28882076 (Homo sapiens)
  • 23840 RGD objects have been annotated to genetic disease  (DOID:630)
  • 24 papers in RGD have been used to annotate PRKCD
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking PRKCD 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:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens) & RGD:12740889|RGD:155967040|RGD:156298716|RGD:329374535|RGD:329378657|RGD:329388303|RGD:401772968|RGD:405670787|RGD:405670794|RGD:405670799|RGD:405670805 (Homo sapiens)
  • 23840 RGD objects have been annotated to genetic disease  (DOID:630)
  • 24 papers in RGD have been used to annotate PRKCD
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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