Gene: RPGRIP1L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L 		0.410 Biomarker group 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 		0.410 Biomarker group 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 		0.410 Biomarker group 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 		0.410 Biomarker group HPO