AtlasTrait
Vertical nystagmus
Vertical nystagmus may present with either up-beating or down-beating eye movements or both. When present in the straight-ahead position of gaze it is referred to as upbeat nystagmus or downbeat nystagmus.
Summary
- Body system
- Abnormality of the eye
AtlasThis 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/vertical-nystagmus.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Vertical nystagmus, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test23 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Familial Hemiplegic MigraineReads 3 of these genesCACNA1AATP1A2SCN1AAbout this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- ECHS1 DeficiencyReads 1 of these genesECHS1About this report →
Show 19 more reports
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- PRR12-Related Neuroocular SyndromeReads 1 of these genesDAGLAAbout this report →
- Hereditary Episodic AtaxiasReads 1 of these genesCACNA1AAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGQPIGNAbout this report →
- Leigh SyndromeReads 3 of these genesNDUFS8ECHS1PET100About this report →
- Epilepsy (Full Panel)Reads 5 of these genesPIGQCACNA1AATP1A2PRRT2SCN1AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesTTBK2CACNA1AAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesNDUFS8ECHS1PET100PEX5TTRAbout this report →
- Hereditary AmyloidosisReads 1 of these genesTTRAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX5About this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesTTBK2CACNA1AMRE11PEX5TMEM106BAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPEX5TMEM106BAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTMEM106BAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesNDUFS8PET100About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPRRT2About this report →
- DNA Repair DiseaseReads 1 of these genesMRE11About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPIGNAbout this report →
Read the genes linked to Vertical nystagmus, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test18 genes linked to Vertical nystagmus
Changes in these genes cause rare conditions in which Vertical nystagmus 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 |
|---|---|---|
| DAGLAdiacylglycerol lipase alpha | Always | In 1 condition |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Always | In 1 condition |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Always | In 1 condition |
| NDUFS8NADH:ubiquinone oxidoreductase core subunit S8 | Always | In 1 condition |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Always | In 1 condition |
| TTBK2tau tubulin kinase 2 | Very often (80–99%) | In 1 condition |
| ALX4ALX homeobox 4 | Often (30–79%) | In 1 condition |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Often (30–79%) | In 2 conditions |
| ECHS1enoyl-CoA hydratase, short chain 1 | Often (30–79%) | In 1 condition |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| MRE11MRE11 double strand break repair nuclease | Sometimes (5–29%) | In 1 condition |
| PET100PET100 cytochrome c oxidase chaperone | Sometimes (5–29%) | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | Sometimes (5–29%) | In 1 condition |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Sometimes (5–29%) | In 1 condition |
| PRRT2proline rich transmembrane protein 2 | Sometimes (5–29%) | In 1 condition |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sometimes (5–29%) | In 1 condition |
| TMEM106Btransmembrane protein 106B | Sometimes (5–29%) | In 1 condition |
| TTRtransthyretin | 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.
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 2026.10.19-9814e911.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Free shipping · Results in 6–8 weeks
