Gene: EPHA2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1969
Gene Symbol: EPHA2
EPHA2 		0.310 GeneticVariation disease BEFREE Our study presented the evidence for a novel EPHA2 kinase domain mutation that causes congenital posterior subcapsular cataracts. 31725171 2019
Entrez Id: 1969
Gene Symbol: EPHA2
EPHA2 		0.310 GermlineCausalMutation disease ORPHANET A novel p.R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family. 23447127 2013
Entrez Id: 1969
Gene Symbol: EPHA2
EPHA2 		0.310 GermlineCausalMutation disease ORPHANET Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract. 19306328 2009