Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6
0.100 Biomarker disease HPO
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
0.010 Biomarker disease BEFREE Our results suggest that ZNF644 may play a role in myopia development. 22539872 2012
Entrez Id: 84627
Gene Symbol: ZNF469
ZNF469
0.100 Biomarker disease HPO
Entrez Id: 79797
Gene Symbol: ZNF408
ZNF408
0.100 Biomarker disease HPO
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
0.100 GeneticVariation disease CLINVAR
Entrez Id: 79698
Gene Symbol: ZMAT4
ZMAT4
0.100 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
0.010 Biomarker disease BEFREE In an experimental mouse model for myopia, we observed significant alterations to gene and protein expression in the retina and sclera of the unilateral induced myopic eyes for Zfhx1b and Sntb1. 23933737 2013
Entrez Id: 643136
Gene Symbol: ZC3H11B
ZC3H11B
0.020 Biomarker disease BEFREE These loci have previously demonstrated association with axial length (ZC3H11B), myopia (NPLOC4), spherical equivalent refractive error (LINC00340) and eye colour (HERC2). 30306274 2018
Entrez Id: 643136
Gene Symbol: ZC3H11B
ZC3H11B
0.020 Biomarker disease BEFREE Association of the <i>ZC3H11B, ZFHX1B</i> and <i>SNTB1</i> genes with myopia of different severities. 31300455 2019
Entrez Id: 9877
Gene Symbol: ZC3H11A
ZC3H11A
0.010 AlteredExpression disease BEFREE In an experimental myopia mouse model, we observed significant alterations to gene and protein expression in the retina and sclera of the unilateral induced myopic eyes for the murine genes ZC3H11A, SLC30A10, and LYPLAL1. 22685421 2012
Entrez Id: 253461
Gene Symbol: ZBTB38
ZBTB38
0.100 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
Entrez Id: 10730
Gene Symbol: YME1L1
YME1L1
0.100 Biomarker disease HPO
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2
0.100 Biomarker disease HPO
Entrez Id: 64131
Gene Symbol: XYLT1
XYLT1
0.100 Biomarker disease HPO
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
0.020 GeneticVariation disease BEFREE WNT7B SNPs located in the same genomic region that includes rs9330813 have previously been associated with CCT in Latinos but with other ocular quantitative traits related to myopia (corneal curvature and axial length) in a Japanese population (rs10453441 and rs200329677). 29847655 2018
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
0.020 AlteredExpression disease BEFREE We also find in a mouse model of myopia downregulation of WNT7B expression in the cornea and upregulation in the retina, suggesting its possible role in the development of myopia. 25823570 2015
Entrez Id: 7482
Gene Symbol: WNT2B
WNT2B
0.010 AlteredExpression disease BEFREE The amounts of Wnt2b, Fzd5 and β-catenin mRNA and protein were significantly greater in form-deprived myopia eyes than in control eyes.DKK-1 (antagonist) reduced the myopic shift in refractive error and increase in axial elongation, whereas Norrin had the opposite effect in FDM eyes. 24755605 2014
Entrez Id: 25861
Gene Symbol: WHRN
WHRN
0.100 Biomarker disease HPO
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
0.100 Biomarker disease HPO
Entrez Id: 57728
Gene Symbol: WDR19
WDR19
0.100 Biomarker disease HPO
Entrez Id: 11169
Gene Symbol: WDHD1
WDHD1
0.010 Biomarker disease BEFREE The purpose is to evaluate the evidence for association between time outdoors and (1) risk of onset of myopia (incident/prevalent myopia); (2) risk of a myopic shift in refractive error and c) risk of progression in myopes only. 28251836 2017
Entrez Id: 51322
Gene Symbol: WAC
WAC
0.100 Biomarker disease HPO
Entrez Id: 157680
Gene Symbol: VPS13B
VPS13B
0.100 Biomarker disease HPO
Entrez Id: 7434
Gene Symbol: VIPR2
VIPR2
0.020 GeneticVariation disease BEFREE The vasoactive intestinal peptide receptor 2 (VIPR2) gene was identified as a myopia susceptibility locus by our group and another group.We continued to fine-map this locus. 31796800 2019
Entrez Id: 7434
Gene Symbol: VIPR2
VIPR2
0.020 AlteredExpression disease BEFREE The VIPR2 and SNTB1 genes are expressed in the retina and the retinal pigment epithelium and have been previously reported to have potential functions for the pathogenesis of myopia. 23406873 2013