eye Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An organ of sight; especially: a nearly spherical hollow organ that is lined with a sensitive retina, is lodged in a bony orbit in the skull, is the vertebrate organ of sight, and is normally paired. (BRENDA Tissue and Enzyme Source Ontology, BTO_0000439)
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Genes

6 genes associated with the disease eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
DENND2A DENN/MADD domain containing 2A
ESRRG estrogen-related receptor gamma
MYH9 myosin, heavy chain 9, non-muscle
PEX14 peroxisomal biogenesis factor 14
SCFD2 sec1 family domain containing 2
TSHR thyroid stimulating hormone receptor