astigmatism Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A refractive error characterized by the optics of the eye to focus a point object into a sharp focused image on the retina, has_symptom blurred vision. (Human Disease Ontology, DOID_11782)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0000483
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Genes

12 genes associated with the astigmatism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PDGFRA platelet-derived growth factor receptor, alpha polypeptide 1.25845
VAX2 ventral anterior homeobox 2 1.12851
DNAH5 dynein, axonemal, heavy chain 5 1.04365
MAML2 mastermind-like 2 (Drosophila) 1.00059
SMPDL3B sphingomyelin phosphodiesterase, acid-like 3B 1.00059
BICC1 BicC family RNA binding protein 1 0.969142
LMO7 LIM domain 7 0.942765
SUCLG2 succinate-CoA ligase, GDP-forming, beta subunit 0.919744
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3 0.919744
CHSY1 chondroitin sulfate synthase 1 0.882984
THSD7B thrombospondin, type I, domain containing 7B 0.868241
USP53 ubiquitin specific peptidase 53 0.855449