Head Tremor Gene Set

Dataset DisGeNET Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An unintentional, oscillating to-and-fro muscle movement affecting head movement. (Human Phenotype Ontology, HP_0002346)
External Link https://www.disgenet.org/browser/0/1/0/C0239882
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21 genes associated with the phenotype Head Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Symbol Name
AFG3L2 AFG3-like AAA ATPase 2
ANO3 anoctamin 3
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CIZ1 CDKN1A interacting zinc finger protein 1
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
DNMT1 DNA (cytosine-5-)-methyltransferase 1
FGF14 fibroblast growth factor 14
GBA2 glucosidase, beta (bile acid) 2
IFRD1 interferon-related developmental regulator 1
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
MTM1 myotubularin 1
NOP56 NOP56 ribonucleoprotein
PEX6 peroxisomal biogenesis factor 6
PIK3R5 phosphoinositide-3-kinase, regulatory subunit 5
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
SCP2 sterol carrier protein 2
SETX senataxin
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase