Myopia Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. (Experimental Factor Ontology, EFO_0003927)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D009216
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Genes

14 genes/proteins associated with the disease Myopia from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
MYP17	myopia 17	2.88009
RDH5	retinol dehydrogenase 5 (11-cis/9-cis)	2.88009
MYP4	myopia 4 (high grade, autosomal dominant)	2.88009
LAMA2	laminin, alpha 2	2.88009
GJD2	gap junction protein, delta 2, 36kDa	2.88009
SIX6	SIX homeobox 6	2.88009
BMP2	bone morphogenetic protein 2	2.88009
COL2A1	collagen, type II, alpha 1	2.88009
RASGRF1	Ras protein-specific guanine nucleotide-releasing factor 1	2.88009
IRX5	iroquois homeobox 5	2.88009
PRSS56	protease, serine, 56	2.88009
COL9A1	collagen, type IX, alpha 1	2.88009
GRIA4	glutamate receptor, ionotropic, AMPA 4	2.88009
KCNQ5	potassium channel, voltage gated KQT-like subfamily Q, member 5	2.88009