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 		0.500 Biomarker group CTD_human The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. 17558409 2007
Entrez Id: 23322
Gene Symbol: RPGRIP1L
RPGRIP1L 		0.500 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 		0.500 Biomarker group GENOMICS_ENGLAND