Gene: RPGR ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.310 Biomarker phenotype CTD_human Moreover, we show that RPGRIP1L interacts biochemically with RPGR, loss of which causes retinal degeneration, and that the Thr229-encoded protein significantly compromises this interaction. 19430481 2009
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.310 Biomarker phenotype LHGDN Mutations in the RPGR gene cause X-linked cone dystrophy. 11875055 2002