Gait Disorders, Neurologic Gene Set

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

8 genes associated with the Gait Disorders, Neurologic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
COMT catechol-O-methyltransferase
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
MT-TK tRNA
MT-TL1 tRNA
TPH1 tryptophan hydroxylase 1
TPH2 tryptophan hydroxylase 2