Trait
Motor tics
Movement-based tics affecting discrete muscle groups.
Summary
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test12 genes linked to Motor tics
Changes in these genes cause rare conditions in which Motor tics 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 |
|---|---|---|
| CEP152centrosomal protein 152 | Often (30–79%) | In 1 condition |
| COASYCoenzyme A synthase | Often (30–79%) | In 1 condition |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Often (30–79%) | In 1 condition |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Often (30–79%) | In 1 condition |
| VPS13Avacuolar protein sorting 13 homolog A | Often (30–79%) | In 1 condition |
| GNB1G protein subunit beta 1 | Sometimes (5–29%) | In 1 condition |
| HNRNPCheterogeneous nuclear ribonucleoprotein C | Sometimes (5–29%) | In 1 condition |
| PANK2pantothenate kinase 2 | Sometimes (5–29%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Rarely (1–4%) | In 1 condition |
| HDChistidine decarboxylase | Not recorded | In 1 condition |
| PTCHD1patched domain containing 1 | Not recorded | In 1 condition |
| SLITRK1SLIT and NTRK like family member 1 | 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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