Tremor, Rubral Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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18 genes associated with the disease Tremor, Rubral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ARCN1 archain 1
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CIT citron rho-interacting serine/threonine kinase
CP ceruloplasmin (ferroxidase)
EGR3 early growth response 3
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRA4 gamma-aminobutyric acid (GABA) A receptor, alpha 4
GK5 glycerol kinase 5 (putative)
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
NPC1 Niemann-Pick disease, type C1
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SOX2 SRY (sex determining region Y)-box 2
UROC1 urocanate hydratase 1