Resting Tremor Gene Set

Dataset DisGeNET Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A resting tremor occurs when muscles are at rest and becomes less noticeable or disappears when the affected muscles are moved. Resting tremors are often slow and coarse. (Human Phenotype Ontology, HP_0002322)
External Link https://www.disgenet.org/browser/0/1/0/C0234379
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Genes

56 genes associated with the phenotype Resting Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Symbol Name
ACHE acetylcholinesterase (Yt blood group)
ADCY5 adenylate cyclase 5
ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
ADORA2A adenosine A2a receptor
ADRB2 adrenoceptor beta 2, surface
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATXN2 ataxin 2
C9ORF72 chromosome 9 open reading frame 72
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CHCHD2 coiled-coil-helix-coiled-coil-helix domain containing 2
CHRM4 cholinergic receptor, muscarinic 4
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DNAJC13 DnaJ (Hsp40) homolog, subfamily C, member 13
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
DNMT1 DNA (cytosine-5-)-methyltransferase 1
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1
FMR1 fragile X mental retardation 1
GBA glucosidase, beta, acid
GIGYF2 GRB10 interacting GYF protein 2
GLUD2 glutamate dehydrogenase 2
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
LRRK2 leucine-rich repeat kinase 2
MAN1B1 mannosidase, alpha, class 1B, member 1
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
MICU1 mitochondrial calcium uptake 1
NR4A2 nuclear receptor subfamily 4, group A, member 2
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PARK2 parkin RBR E3 ubiquitin protein ligase
PINK1 PTEN induced putative kinase 1
PODXL podocalyxin-like
POLG polymerase (DNA directed), gamma
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
RAB39B RAB39B, member RAS oncogene family
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCAIP synuclein, alpha interacting protein
SPG11 spastic paraplegia 11 (autosomal recessive)
SYNJ1 synaptojanin 1
TAF1 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
TBP TATA box binding protein
TRH thyrotropin-releasing hormone
TWNK twinkle mtDNA helicase
VPS13C vacuolar protein sorting 13 homolog C (S. cerevisiae)
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)