Gene: LCA5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 167691
Gene Symbol: LCA5
LCA5 		0.100 CausalMutation group CLINVAR Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. 18000884 2007
Entrez Id: 167691
Gene Symbol: LCA5
LCA5 		0.100 CausalMutation group CLINVAR Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. 17546029 2007
Entrez Id: 167691
Gene Symbol: LCA5
LCA5 		0.100 CausalMutation group CLINVAR Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus. 12642313 2003
Entrez Id: 167691
Gene Symbol: LCA5
LCA5 		0.100 CausalMutation group CLINVAR A novel locus for Leber congenital amaurosis maps to chromosome 6q. 10631161 2000