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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking DPEP2 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:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens) & RGD:155911586|RGD:156038110|RGD:156065405|RGD:156101994|RGD:156105458|RGD:156169240|RGD:156182068|RGD:156227942|RGD:156241888|RGD:156268742|RGD:156358453|RGD:156385305|RGD:156395510|RGD:329382816|RGD:329388212|RGD:329391767|RGD:401731723|RGD:401762423|RGD:401773077|RGD:401874225|RGD:401891497 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 3 papers in RGD have been used to annotate DPEP2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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