Gene: CERKL ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 375298
Gene Symbol: CERKL
CERKL 		0.020 GeneticVariation phenotype LHGDN This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease. 18978954 2008
Entrez Id: 375298
Gene Symbol: CERKL
CERKL 		0.020 GeneticVariation phenotype LHGDN A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews. 18055789 2007