Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 PosttranslationalModification disease BEFREE Finally, we demonstrate that genetic inactivation of Prss56 rescues axial elongation in a mouse model of myopia caused by a null mutation in Egr1. 29529029 2018
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 GeneticVariation disease BEFREE We also found evidence of association with spherical equivalent on 2q37.1 in PRSS56 at rs1550094 (MAF = 31%, β = -0.33, p = 1.7 × 10(-3)), a region previously associated with myopia. 27440996 2016
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 GeneticVariation disease BEFREE Two recent large-scale genome-wide association studies identified significant associations between myopia and single nucleotide polymorphisms (SNPs) near the PRSS56, BMP3, KCNQ5, LAMA2, TOX, TJP2, RDH5, ZIC2, RASGRF1, GJD2, RBFOX1, and SHISA6 genes. 25587058 2015
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 GeneticVariation disease BEFREE Transcripts of Prss56, a gene associated with angle-closure glaucoma, posterior microphthalmia and myopia, were increased in Mfrprd6 eyes by 17-fold. 25357075 2014
Entrez Id: 646960
Gene Symbol: PRSS56
PRSS56
0.440 Biomarker disease CTD_human Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134 2013