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Trait
Horizontal nystagmus
Nystagmus consisting of horizontal to-and-fro eye movements.
Summary
- Also called
- Nystagmus, horizontal
- Body system
- Abnormality of the eye
Horizontal nystagmusHP:0000666
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Read the genes linked to Horizontal nystagmus, and the rest of your genome, with one test.
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Get my Genome Test105 genes linked to Horizontal nystagmus
Changes in these genes cause rare conditions in which Horizontal 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 |
|---|---|---|
| AHRaryl hydrocarbon receptor | Always | In 1 condition |
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Always | In 1 condition |
| AP3B1adaptor related protein complex 3 subunit beta 1 | Always | In 1 condition |
| ASH1LASH1 like histone lysine methyltransferase | Always | In 1 condition |
| ATG5autophagy related 5 | Always | In 1 condition |
| CCT3chaperonin containing TCP1 subunit 3 | Always | In 1 condition |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Always | In 1 condition |
| COQ5coenzyme Q5, methyltransferase | Always | In 1 condition |
| COX15cytochrome c oxidase assembly factor COX15 | Always | In 1 condition |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Always | In 1 condition |
| DNM1Ldynamin 1L | Always | In 1 condition |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Always | In 1 condition |
| EXOSC5exosome component 5 | Always | In 1 condition |
| FDXRferredoxin reductase | Always | In 1 condition |
| GATA3GATA binding protein 3 | Always | In 1 condition |
| GMPPAGDP-mannose pyrophosphorylase A | Always | In 1 condition |
| HARS1histidyl-tRNA synthetase 1 | Always | In 1 condition |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Always | In 1 condition |
| KDM6Blysine demethylase 6B | Always | In 1 condition |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Always | In 1 condition |
| MMADHCmetabolism of cobalamin associated D | Always | In 1 condition |
| MRPL12mitochondrial ribosomal protein L12 | Always | In 1 condition |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Always | In 1 condition |
| NOTCH3notch receptor 3 | Always | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Always | In 1 condition |
| PSAPprosaposin | Always | In 1 condition |
| RAB3ARAB3A, member RAS oncogene family | Always | In 1 condition |
| UBA5ubiquitin like modifier activating enzyme 5 | Always | In 1 condition |
| XRCC1X-ray repair cross complementing 1 | Always | In 1 condition |
| GPR143G protein-coupled receptor 143 | Very often (80–99%) | In 1 condition |
| KIF1Ckinesin family member 1C | Very often (80–99%) | In 2 conditions |
| MAB21L1mab-21 like 1 | Very often (80–99%) | In 2 conditions |
| TTBK2tau tubulin kinase 2 | Very often (80–99%) | In 1 condition |
| ALX4ALX homeobox 4 | Often (30–79%) | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Often (30–79%) | In 1 condition |
| COL18A1collagen type XVIII alpha 1 chain | Often (30–79%) | In 1 condition |
| CWF19L1CWF19 like cell cycle control factor 1 | Often (30–79%) | In 1 condition |
| DAB1DAB adaptor protein 1 | Often (30–79%) | In 1 condition |
| DAGLAdiacylglycerol lipase alpha | Often (30–79%) | In 1 condition |
| EXOSC9exosome component 9 | Often (30–79%) | In 1 condition |
Show 65 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| FA2Hfatty acid 2-hydroxylase | Often (30–79%) | In 1 condition |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Often (30–79%) | In 2 conditions |
| GRM6glutamate metabotropic receptor 6 | Often (30–79%) | In 1 condition |
| HMX1H6 family homeobox 1 | Often (30–79%) | In 1 condition |
| HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 | Often (30–79%) | In 1 condition |
| KIF5Akinesin family member 5A | Often (30–79%) | In 1 condition |
| KLC4kinesin light chain 4 | Often (30–79%) | In 1 condition |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Often (30–79%) | In 2 conditions |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Often (30–79%) | In 1 condition |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Often (30–79%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Often (30–79%) | In 1 condition |
| POLR3BRNA polymerase III subunit B | Often (30–79%) | In 1 condition |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Often (30–79%) | In 1 condition |
| RBL2RB transcriptional corepressor like 2 | Often (30–79%) | In 1 condition |
| SLC18A3solute carrier family 18 member A3 | Often (30–79%) | In 1 condition |
| SLC35B2solute carrier family 35 member B2 | Often (30–79%) | In 1 condition |
| SPTBN4spectrin beta, non-erythrocytic 4 | Often (30–79%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Often (30–79%) | In 2 conditions |
| TPP1tripeptidyl peptidase 1 | Often (30–79%) | In 1 condition |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Often (30–79%) | In 1 condition |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Often (30–79%) | In 1 condition |
| ZNF408zinc finger protein 408 | Often (30–79%) | In 1 condition |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Sometimes (5–29%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sometimes (5–29%) | In 1 condition |
| ANO10anoctamin 10 | Sometimes (5–29%) | In 1 condition |
| CHD8chromodomain helicase DNA binding protein 8 | Sometimes (5–29%) | In 1 condition |
| DPP6dipeptidyl peptidase like 6 | Sometimes (5–29%) | In 1 condition |
| ERLIN2ER lipid raft associated 2 | Sometimes (5–29%) | In 1 condition |
| GCH1GTP cyclohydrolase 1 | Sometimes (5–29%) | In 1 condition |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Sometimes (5–29%) | In 1 condition |
| IMPDH2inosine monophosphate dehydrogenase 2 | Sometimes (5–29%) | In 1 condition |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Sometimes (5–29%) | In 1 condition |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Sometimes (5–29%) | In 1 condition |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| LYSTlysosomal trafficking regulator | Sometimes (5–29%) | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Sometimes (5–29%) | In 1 condition |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Sometimes (5–29%) | In 1 condition |
| NFIXnuclear factor I X | Sometimes (5–29%) | In 1 condition |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Sometimes (5–29%) | In 1 condition |
| OPA1OPA1 mitochondrial dynamin like GTPase | Sometimes (5–29%) | In 2 conditions |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| PET100PET100 cytochrome c oxidase chaperone | Sometimes (5–29%) | In 1 condition |
| PEX16peroxisomal biogenesis factor 16 | Sometimes (5–29%) | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | Sometimes (5–29%) | In 1 condition |
| PLP1proteolipid protein 1 | Sometimes (5–29%) | In 1 condition |
| SPTBN2spectrin beta, non-erythrocytic 2 | Sometimes (5–29%) | In 1 condition |
| STUB1STIP1 homology and U-box containing protein 1 | Sometimes (5–29%) | In 1 condition |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Sometimes (5–29%) | In 1 condition |
| TAF2TATA-box binding protein associated factor 2 | Sometimes (5–29%) | In 1 condition |
| TMEM106Btransmembrane protein 106B | Sometimes (5–29%) | In 1 condition |
| TMEM126Atransmembrane protein 126A | Sometimes (5–29%) | In 1 condition |
| TTRtransthyretin | Sometimes (5–29%) | In 1 condition |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Not recorded | In 1 condition |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Not recorded | In 1 condition |
| FRMD7FERM domain containing 7 | Not recorded | In 1 condition |
| GBA1glucosylceramidase beta 1 | Not recorded | In 1 condition |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Not recorded | In 1 condition |
| HPS4HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 | Not recorded | In 1 condition |
| HPS5HPS5 biogenesis of lysosomal organelles complex 2 subunit 2 | Not recorded | In 1 condition |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Not recorded | In 1 condition |
| KCNV2potassium voltage-gated channel modifier subfamily V member 2 | Not recorded | In 1 condition |
| SIX6SIX homeobox 6 | Not recorded | In 1 condition |
| SNIP1Smad nuclear interacting protein 1 | Not recorded | In 1 condition |
| SURF1SURF1 cytochrome c oxidase assembly factor | 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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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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Log InAskGet Startedfrom $449
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks