Trait
Abnormal vestibular function
An abnormality of the functioning of the vestibular apparatus.
Summary
- Also called
- Impaired vestibular function, Interictal vestibular dysfunction, Vestibular function defect
- Body system
- Abnormality of the ear
Reference genomeGRCh38hg38
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Get my Genome Test38 genes linked to Abnormal vestibular function
Changes in these genes cause rare conditions in which Abnormal vestibular function 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 |
|---|---|---|
| CLIC5CLIC family member 5 | Always | In 1 condition |
| ESPNespin | Always | In 2 conditions |
| TMEM132Etransmembrane protein 132E | Always | In 1 condition |
| PCDH15protocadherin related 15 | Very often (80–99%) | In 3 conditions |
| CDH23cadherin related 23 | Often (30–79%) | In 2 conditions |
| CLRN1clarin 1 | Often (30–79%) | In 2 conditions |
| COCHcochlin | Often (30–79%) | In 1 condition |
| MYO7Amyosin VIIA | Often (30–79%) | In 4 conditions |
| POLGDNA polymerase gamma, catalytic subunit | Often (30–79%) | In 2 conditions |
| SLC39A14solute carrier family 39 member 14 | Often (30–79%) | In 1 condition |
| TIMM8Atranslocase of inner mitochondrial membrane 8A | Often (30–79%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Often (30–79%) | In 2 conditions |
| USH1CUSH1 protein network component harmonin | Often (30–79%) | In 1 condition |
| USH1GUSH1 protein network component sans | Often (30–79%) | In 2 conditions |
| ALMS1ALMS1 centrosome and basal body associated protein | Sometimes (5–29%) | In 1 condition |
| ARSGarylsulfatase G | Sometimes (5–29%) | In 1 condition |
| ATXN3ataxin 3 | Sometimes (5–29%) | In 3 conditions |
| CEP78centrosomal protein 78 | Sometimes (5–29%) | In 1 condition |
| GJB2gap junction protein beta 2 | Sometimes (5–29%) | In 1 condition |
| GJB3gap junction protein beta 3 | Sometimes (5–29%) | In 1 condition |
| GJB6gap junction protein beta 6 | Sometimes (5–29%) | In 2 conditions |
| HARS1histidyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| JAG1jagged canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Sometimes (5–29%) | In 1 condition |
| MYO6myosin VI | Sometimes (5–29%) | In 1 condition |
| PSAPprosaposin | Sometimes (5–29%) | In 1 condition |
| SOX6SRY-box transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| ADGRV1adhesion G protein-coupled receptor V1 | Rarely (1–4%) | In 1 condition |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Rarely (1–4%) | In 1 condition |
| PDZD7PDZ domain containing 7 | Rarely (1–4%) | In 1 condition |
| USH2Ausherin | Rarely (1–4%) | In 1 condition |
| WHRNwhirlin | Rarely (1–4%) | In 1 condition |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Not recorded | In 1 condition |
| CIB2calcium and integrin binding family member 2 | Not recorded | In 1 condition |
| FOXI1forkhead box I1 | Not recorded | In 1 condition |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Not recorded | In 1 condition |
| PTPRQprotein tyrosine phosphatase receptor type Q | Not recorded | In 1 condition |
| SLC26A4solute carrier family 26 member 4 | 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.
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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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