Intention Tremor Gene Set

Dataset DisGeNET Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A type of kinetic tremor that occurs during target directed movement is called intention tremor. That is, an oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient's nose or a physician's finger). (Human Phenotype Ontology, HP_0002080)
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20 genes associated with the phenotype Intention Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
AFG3L2 AFG3-like AAA ATPase 2
ATXN2 ataxin 2
ATXN3 ataxin 3
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CUL4B cullin 4B
ERCC8 excision repair cross-complementation group 8
FIG4 FIG4 phosphoinositide 5-phosphatase
FMR1 fragile X mental retardation 1
GJC2 gap junction protein, gamma 2, 47kDa
LY6E lymphocyte antigen 6 complex, locus E
MAOA monoamine oxidase A
MECP2 methyl CpG binding protein 2
PPP1R15B protein phosphatase 1, regulatory subunit 15B
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PYROXD1 pyridine nucleotide-disulphide oxidoreductase domain 1
SCYL1 SCY1-like 1 (S. cerevisiae)
SLC6A17 solute carrier family 6 (neutral amino acid transporter), member 17
UBE3A ubiquitin protein ligase E3A
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial