Ocular Motility Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

9 genes associated with the Ocular Motility Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
ERBB4 erb-b2 receptor tyrosine kinase 4
GRM3 glutamate receptor, metabotropic 3
NRG1 neuregulin 1
NRG3 neuregulin 3
RTN4R reticulon 4 receptor
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3