myopia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A refractive error characterized by the inability to see farther objects clearly. (Human Disease Ontology, DOID_11830)
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39 genes associated with the disease myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACTC1 actin, alpha, cardiac muscle 1
BDNF brain-derived neurotrophic factor
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CHRM1 cholinergic receptor, muscarinic 1
COL18A1 collagen, type XVIII, alpha 1
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CTNND2 catenin (cadherin-associated protein), delta 2
EGR1 early growth response 1
EPYC epiphycan
FGF2 fibroblast growth factor 2 (basic)
FMOD fibromodulin
GJD2 gap junction protein, delta 2, 36kDa
GRM6 glutamate receptor, metabotropic 6
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
IGF1 insulin-like growth factor 1 (somatomedin C)
IRX1 iroquois homeobox 1
IRX2 iroquois homeobox 2
LUM lumican
MET MET proto-oncogene, receptor tyrosine kinase
MIPEP mitochondrial intermediate peptidase
MMP1 matrix metallopeptidase 1
MMP2 matrix metallopeptidase 2
MMP3 matrix metallopeptidase 3
MYOC myocilin, trabecular meshwork inducible glucocorticoid response
OPTC opticin
PAPD7 PAP associated domain containing 7
PAX6 paired box 6
PRPH peripherin
RARB retinoic acid receptor, beta
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
RDH8 retinol dehydrogenase 8 (all-trans)
SOX2 SRY (sex determining region Y)-box 2
TGFB1 transforming growth factor, beta 1
TGFB2 transforming growth factor, beta 2
TGIF1 TGFB-induced factor homeobox 1
UMODL1 uromodulin-like 1
ZNF831 zinc finger protein 831