Hyperhidrosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormal excessive perspiration (sweating). (Human Phenotype Ontology, HP_0000975)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006945
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Genes

19 genes/proteins associated with the disease Hyperhidrosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.63473
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.60151
PRL prolactin 1.51835
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.31506
KCNJ3 potassium channel, inwardly rectifying subfamily J, member 3 1.30971
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6 1.30512
CAT catalase 1.28058
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.21468
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19 1.12973
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.11809
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.11536
GDPD3 glycerophosphodiester phosphodiesterase domain containing 3 1.10838
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3 1.09611
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 1.06406
FABP1 fatty acid binding protein 1, liver 1.05349
CRH corticotropin releasing hormone 1.04904
SERPINA3 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3 1.02596
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.02299
HMGCS1 3-hydroxy-3-methylglutaryl-CoA synthase 1 (soluble) 1.0204