Gene: RCC1L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81554
Gene Symbol: RCC1L
RCC1L 		0.020 Biomarker disease BEFREE Clinical research into mutations of the RPGR gene showed that lack of either the RCC1-like domain of the ORF15 causes X-linked retinitis pigmentosa. 17249551 2006
Entrez Id: 81554
Gene Symbol: RCC1L
RCC1L 		0.020 GeneticVariation disease BEFREE To describe a macrodeletion spanning entire RCC1-like doman in the RPGR gene in one Japanese family with X-linked retinitis pigmentosa (XLRP). 16052169 2005