Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 368
Gene Symbol: ABCC6
ABCC6 		0.100 Biomarker disease HPO
Entrez Id: 51
Gene Symbol: ACOX1
ACOX1 		0.100 Biomarker disease HPO
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.100 Biomarker disease HPO
Entrez Id: 170691
Gene Symbol: ADAMTS17
ADAMTS17 		0.100 Biomarker disease HPO
Entrez Id: 170692
Gene Symbol: ADAMTS18
ADAMTS18 		0.010 GeneticVariation disease BEFREE Our data suggest that ADAMTS18 plays an essential role in early eye development and that mutations therein cause a distinct eye phenotype that is mainly characterized by microcornea and myopia. 23818446 2013
Entrez Id: 9509
Gene Symbol: ADAMTS2
ADAMTS2 		0.110 Biomarker disease BEFREE These included FBN1, ADAMTS2 and TGFB2 which associate with connective tissue disorders (Marfan, Ehlers-Danlos and Loeys-Dietz syndromes), and the LUM-DCN-KERA gene complex involved in myopia, corneal dystrophies and cornea plana. 29760442 2018
Entrez Id: 9509
Gene Symbol: ADAMTS2
ADAMTS2 		0.110 Biomarker disease HPO
Entrez Id: 92949
Gene Symbol: ADAMTSL1
ADAMTSL1 		0.100 Biomarker disease HPO
Entrez Id: 92949
Gene Symbol: ADAMTSL1
ADAMTSL1 		0.100 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
Entrez Id: 84059
Gene Symbol: ADGRV1
ADGRV1 		0.100 Biomarker disease HPO
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.210 Biomarker disease MGD Adenosine A2A, but not A1, receptors mediate the arousal effect of caffeine. 15965471 2005
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.210 Biomarker disease MGD A(2A) adenosine receptor deficiency attenuates brain injury induced by transient focal ischemia in mice. 10531422 1999
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.210 GeneticVariation disease BEFREE Genetic deletion of the adenosine A2A receptor confers postnatal development of relative myopia in mice. 20484596 2010
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.210 Biomarker disease MGD Genetic deletion of the adenosine A2A receptor confers postnatal development of relative myopia in mice. 20484596 2010
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.210 Biomarker disease MGD Selective attenuation of psychostimulant-induced behavioral responses in mice lacking A(2A) adenosine receptors. 10771351 2000
Entrez Id: 146
Gene Symbol: ADRA1D
ADRA1D 		0.010 GeneticVariation disease BEFREE Single nucleotide polymorphisms (SNPs) at the type I collagen alpha-1 gene (COL1A1) may cause different susceptibilities to myopia. 17273809 2007
Entrez Id: 60509
Gene Symbol: AGBL5
AGBL5 		0.100 Biomarker disease HPO
Entrez Id: 55750
Gene Symbol: AGK
AGK 		0.100 Biomarker disease HPO
Entrez Id: 207
Gene Symbol: AKT1
AKT1 		0.100 Biomarker disease HPO
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1 		0.100 Biomarker disease HPO
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2 		0.100 Biomarker disease HPO
Entrez Id: 241
Gene Symbol: ALOX5AP
ALOX5AP 		0.020 Biomarker disease BEFREE INVERTED INTERNAL LIMITING MEMBRANE FLAP TECHNIQUE FOR TREATMENT OF MACULAR HOLE RETINAL DETACHMENT IN HIGHLY MYOPIC EYES. 29065014 2018
Entrez Id: 241
Gene Symbol: ALOX5AP
ALOX5AP 		0.020 Biomarker disease BEFREE EFFICACY OF THE INVERTED INTERNAL LIMITING MEMBRANE FLAP TECHNIQUE WITH VITRECTOMY FOR RETINAL DETACHMENT ASSOCIATED WITH MYOPIC MACULAR HOLES. 28225722 2017
Entrez Id: 262
Gene Symbol: AMD1
AMD1 		0.020 GeneticVariation disease BEFREE Evaluation of 10 AMD Associated Polymorphisms as a Cause of Choroidal Neovascularization in Highly Myopic Eyes. 27643879 2016