Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.410 Biomarker CTD_human In addition, we show that RPGRIP1L colocalizes at the basal body and centrosomes with the protein products of both NPHP6 and NPHP4, known genes associated with MKS, CORS and nephronophthisis (a related renal disorder and ciliopathy). 17558409

2007

Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.410 Biomarker BEFREE In addition, we show that RPGRIP1L colocalizes at the basal body and centrosomes with the protein products of both NPHP6 and NPHP4, known genes associated with MKS, CORS and nephronophthisis (a related renal disorder and ciliopathy). 17558409

2007

Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.410 Biomarker CTD_human Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome. 17558407

2007

Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.410 Biomarker HPO