Trait
Hand tremor
An unintentional, oscillating to-and-fro muscle movement affecting the hand.
Summary
- Also called
- Tremor of hand, Tremor of hands, tremors in hands
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test51 genes linked to Hand tremor
Changes in these genes cause rare conditions in which Hand 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 |
|---|---|---|
| ATP7BATPase copper transporting beta | Always | In 1 condition |
| GTPBP1GTP binding protein 1 | Always | In 1 condition |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Always | In 1 condition |
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| RAB32RAB32, member RAS oncogene family | Always | In 1 condition |
| RAB3ARAB3A, member RAS oncogene family | Always | In 1 condition |
| SLC6A17solute carrier family 6 member 17 | Always | In 2 conditions |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Always | In 1 condition |
| TOR1Atorsin family 1 member A | Always | In 1 condition |
| ADRA2Badrenoceptor alpha 2B | Very often (80–99%) | In 1 condition |
| CNTN2contactin 2 | Very often (80–99%) | In 1 condition |
| CTNND2catenin delta 2 | Very often (80–99%) | In 1 condition |
| MARCHF6membrane associated ring-CH-type finger 6 | Very often (80–99%) | In 1 condition |
| PDK3pyruvate dehydrogenase kinase 3 | Very often (80–99%) | In 2 conditions |
| RAPGEF2Rap guanine nucleotide exchange factor 2 | Very often (80–99%) | In 1 condition |
| SAMD12sterile alpha motif domain containing 12 | Very often (80–99%) | In 1 condition |
| SMN1survival of motor neuron 1, telomeric | Very often (80–99%) | In 3 conditions |
| TBC1D24TBC1 domain family member 24 | Very often (80–99%) | In 1 condition |
| TNRC6Atrinucleotide repeat containing adaptor 6A | Very often (80–99%) | In 1 condition |
| TSHRthyroid stimulating hormone receptor | Very often (80–99%) | In 2 conditions |
| YEATS2YEATS domain containing 2 | Very often (80–99%) | In 1 condition |
| CAMTA1calmodulin binding transcription activator 1 | Often (30–79%) | In 1 condition |
| GCKglucokinase | Often (30–79%) | In 1 condition |
| GJB1gap junction protein beta 1 | Often (30–79%) | In 1 condition |
| GTPBP2GTP binding protein 2 | Often (30–79%) | In 1 condition |
| MARS1methionyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| MFN2mitofusin 2 | Often (30–79%) | In 1 condition |
| NEFLneurofilament light chain | Often (30–79%) | In 1 condition |
| NGFnerve growth factor | Often (30–79%) | In 1 condition |
| PLA2G6phospholipase A2 group VI | Often (30–79%) | In 1 condition |
| PMP2peripheral myelin protein 2 | Often (30–79%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Often (30–79%) | In 1 condition |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Often (30–79%) | In 1 condition |
| TAF1TATA-box binding protein associated factor 1 | Often (30–79%) | In 1 condition |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Often (30–79%) | In 1 condition |
| VRK1VRK serine/threonine kinase 1 | Often (30–79%) | In 1 condition |
| ZFRzinc finger RNA binding protein | Often (30–79%) | In 1 condition |
| AARS2alanyl-tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| ANO3anoctamin 3 | Sometimes (5–29%) | In 1 condition |
| ERLIN2ER lipid raft associated 2 | Sometimes (5–29%) | In 2 conditions |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| FGF14fibroblast growth factor 14 | Sometimes (5–29%) | In 1 condition |
| GBA2glucosylceramidase beta 2 | Sometimes (5–29%) | In 1 condition |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Sometimes (5–29%) | In 1 condition |
| STUB1STIP1 homology and U-box containing protein 1 | Sometimes (5–29%) | In 1 condition |
| TFGtrafficking from ER to golgi regulator | Sometimes (5–29%) | In 1 condition |
| ZFYVE26zinc finger FYVE-type containing 26 | Sometimes (5–29%) | In 1 condition |
| NOP56NOP56 ribonucleoprotein | Rarely (1–4%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Rarely (1–4%) | In 1 condition |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Not recorded | In 1 condition |
| DRD3dopamine receptor D3 | Not recorded | In 1 condition |
| SMN2survival of motor neuron 2, centromeric | 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.
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 2026.10.16-c6eea6bf.
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