Gene: OCRL ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4952
Gene Symbol: OCRL
OCRL 		0.110 GeneticVariation disease BEFREE Genotype-phenotype correlation of OCRL1 mutations associated with congenital glaucoma revealed clustering of missense and deletion mutations in the 5-phosphatase domain and the RhoGAP-like domain. 28473699 2017
Entrez Id: 4952
Gene Symbol: OCRL
OCRL 		0.110 Biomarker disease HPO