Trait
Titubation
Nodding movement of the head or body.
Summary
- 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 Test8 genes linked to Titubation
Changes in these genes cause rare conditions in which Titubation 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 |
|---|---|---|
| GTPBP2GTP binding protein 2 | Always | In 1 condition |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Often (30–79%) | In 1 condition |
| KIF1Ckinesin family member 1C | Often (30–79%) | In 1 condition |
| PLP1proteolipid protein 1 | Often (30–79%) | In 2 conditions |
| IFRD1interferon related developmental regulator 1 | Sometimes (5–29%) | In 1 condition |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Sometimes (5–29%) | In 1 condition |
| MAGmyelin associated glycoprotein | Sometimes (5–29%) | In 1 condition |
| PITRM1pitrilysin metallopeptidase 1 | Sometimes (5–29%) | 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.
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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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