Cyclothymic Disorder Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A bipolar disorder that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes. (Human Disease Ontology, DOID_845)
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Genes

6 genes associated with the Cyclothymic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AKR1C4 aldo-keto reductase family 1, member C4
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
OXTR oxytocin receptor
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SRD5A1 steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)