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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking RPGRIP1L and cystic kidney disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • 24 additional annotations were made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • 230 RGD objects have been annotated to cystic kidney disease  (DOID:2975)
  • 8 papers in RGD have been used to annotate RPGRIP1L
  • Curation Notes: associated with Meckel Syndrome, Type 5;DNA:mutations:exons:


  • An association has been curated linking Rpgrip1l and cystic kidney disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • The annotation has been inferred from sequence orthology with RPGRIP1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 24 additional annotations were made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • 230 RGD objects have been annotated to cystic kidney disease  (DOID:2975)
  • 11 papers in RGD have been used to annotate Rpgrip1l
  • Curation Notes: associated with Meckel Syndrome, Type 5;DNA:mutations:exons:


  • An association has been curated linking Rpgrip1l and cystic kidney disease in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • The annotation has been inferred from sequence orthology with RPGRIP1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 24 additional annotations were made from Delous M, etal., Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.
  • 230 RGD objects have been annotated to cystic kidney disease  (DOID:2975)
  • 10 papers in RGD have been used to annotate Rpgrip1l
  • Curation Notes: associated with Meckel Syndrome, Type 5;DNA:mutations:exons:


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