Myopia Gene Set

Dataset CTD 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)
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