AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Trait
Resting tremor
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.
Summary
- Also called
- Tremor at rest, Rest tremor
- Body system
- Abnormality of the nervous system
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/resting-tremor.json"
page <- fromJSON(url)
page$trait$nameResting tremorHP:0002322
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Read the genes linked to Resting tremor, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test61 genes linked to Resting tremor
Changes in these genes cause rare conditions in which Resting tremor is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ATP6AP2ATPase H+ transporting accessory protein 2 | Always | In 2 conditions |
| EPG5ectopic P-granules 5 autophagy tethering factor | Always | In 1 condition |
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Always | In 2 conditions |
| VPS13Cvacuolar protein sorting 13 homolog C | Always | In 1 condition |
| CHCHD2coiled-coil-helix-coiled-coil-helix domain containing 2 | Very often (80–99%) | In 1 condition |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Very often (80–99%) | In 1 condition |
| PODXLpodocalyxin like | Very often (80–99%) | In 1 condition |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Very often (80–99%) | In 1 condition |
| RAB39BRAB39B, member RAS oncogene family | Very often (80–99%) | In 1 condition |
| SYNJ1synaptojanin 1 | Very often (80–99%) | In 1 condition |
| ADCY5adenylate cyclase 5 | Often (30–79%) | In 2 conditions |
| COQ2coenzyme Q2, polyprenyltransferase | Often (30–79%) | In 2 conditions |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Often (30–79%) | In 1 condition |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Often (30–79%) | In 2 conditions |
| FBXO7F-box protein 7 | Often (30–79%) | In 1 condition |
| GBA1glucosylceramidase beta 1 | Often (30–79%) | In 2 conditions |
| GIGYF2GRB10 interacting GYF protein 2 | Often (30–79%) | In 2 conditions |
| LRRK2leucine rich repeat kinase 2 | Often (30–79%) | In 2 conditions |
| MICU1mitochondrial calcium uptake 1 | Often (30–79%) | In 1 condition |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Often (30–79%) | In 2 conditions |
| PLA2G6phospholipase A2 group VI | Often (30–79%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Often (30–79%) | In 2 conditions |
| POLG2DNA polymerase gamma 2, accessory subunit | Often (30–79%) | In 1 condition |
| PRKNparkin RBR E3 ubiquitin protein ligase | Often (30–79%) | In 1 condition |
| PSAPprosaposin | Often (30–79%) | In 1 condition |
| PTPAprotein phosphatase 2 phosphatase activator | Often (30–79%) | In 1 condition |
| RAB32RAB32, member RAS oncogene family | Often (30–79%) | In 1 condition |
| RAB3ARAB3A, member RAS oncogene family | Often (30–79%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Often (30–79%) | In 1 condition |
| SLC25A4solute carrier family 25 member 4 | Often (30–79%) | In 1 condition |
| SLC9A6solute carrier family 9 member A6 | Often (30–79%) | In 1 condition |
| SNCAsynuclein alpha | Often (30–79%) | In 2 conditions |
| TAF1TATA-box binding protein associated factor 1 | Often (30–79%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Often (30–79%) | In 1 condition |
| UQCRC1ubiquinol-cytochrome c reductase core protein 1 | Often (30–79%) | In 1 condition |
| VPS35VPS35 retromer complex component | Often (30–79%) | In 2 conditions |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sometimes (5–29%) | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Sometimes (5–29%) | In 1 condition |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
Show 21 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Sometimes (5–29%) | In 1 condition |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Sometimes (5–29%) | In 1 condition |
| DNMT1DNA methyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| GCH1GTP cyclohydrolase 1 | Sometimes (5–29%) | In 1 condition |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Sometimes (5–29%) | In 1 condition |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Sometimes (5–29%) | In 1 condition |
| PARK7Parkinsonism associated deglycase | Sometimes (5–29%) | In 1 condition |
| TTC19tetratricopeptide repeat domain 19 | Sometimes (5–29%) | In 1 condition |
| VPS13Avacuolar protein sorting 13 homolog A | Sometimes (5–29%) | In 1 condition |
| FTLferritin light chain | Rarely (1–4%) | In 1 condition |
| MAN1B1mannosidase alpha class 1B member 1 | Rarely (1–4%) | In 1 condition |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Not recorded | In 1 condition |
| ATXN2ataxin 2 | Not recorded | In 1 condition |
| ATXN3ataxin 3 | Not recorded | In 1 condition |
| ATXN8OSATXN8 opposite strand lncRNA | Not recorded | In 1 condition |
| FMR1fragile X messenger ribonucleoprotein 1 | Not recorded | In 1 condition |
| MAPTmicrotubule associated protein tau | Not recorded | In 1 condition |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Not recorded | In 1 condition |
| PINK1PTEN induced kinase 1 | Not recorded | In 1 condition |
| SNCAIPsynuclein alpha interacting protein | Not recorded | In 1 condition |
| TBPTATA-box binding protein | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks