Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2301
Gene Symbol: FOXE3
FOXE3 		0.010 GeneticVariation disease BEFREE The identification of 2 novel pathogenic variants in our patients expands the mutational spectrum in FOXE3-related congenital eye disorders. 29878917 2018
Entrez Id: 7101
Gene Symbol: NR2E1
NR2E1 		0.010 Biomarker disease BEFREE Nuclear receptor 2E1 (NR2E1) is a transcription factor with many roles during eye development and thus may be responsible for the occurrence of certain congenital eye disorders in humans. 23213277 2012