Trait
Pendular nystagmus
Rhythmic, involuntary sinusoidal oscillations of one or both eyes. The waveform of pendular nystagmus may occur in any direction.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test35 genes linked to Pendular nystagmus
Changes in these genes cause rare conditions in which Pendular 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 |
| GFAPglial fibrillary acidic protein | Always | In 1 condition |
| HMGB3high mobility group box 3 | Always | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Always | In 1 condition |
| SDHDsuccinate dehydrogenase complex subunit D | Always | In 1 condition |
| TMEM63Atransmembrane protein 63A | Always | In 1 condition |
| ATF6activating transcription factor 6 | Very often (80–99%) | In 1 condition |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Very often (80–99%) | In 1 condition |
| CNGA3cyclic nucleotide gated channel subunit alpha 3 | Very often (80–99%) | In 2 conditions |
| CNGB3cyclic nucleotide gated channel subunit beta 3 | Very often (80–99%) | In 1 condition |
| GNAT2G protein subunit alpha transducin 2 | Very often (80–99%) | In 1 condition |
| PDE6Cphosphodiesterase 6C | Very often (80–99%) | In 1 condition |
| PDE6Hphosphodiesterase 6H | Very often (80–99%) | In 1 condition |
| RPGRretinitis pigmentosa GTPase regulator | Very often (80–99%) | In 1 condition |
| CNNM4cyclin and CBS domain divalent metal cation transport mediator 4 | Often (30–79%) | In 1 condition |
| DLATdihydrolipoamide S-acetyltransferase | Often (30–79%) | In 1 condition |
| NT5C25'-nucleotidase, cytosolic II | Often (30–79%) | In 1 condition |
| PLP1proteolipid protein 1 | Often (30–79%) | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| DNMBPdynamin binding protein | Sometimes (5–29%) | In 1 condition |
| OPN1SWopsin 1, short wave sensitive | Sometimes (5–29%) | In 1 condition |
| PEX2peroxisomal biogenesis factor 2 | Sometimes (5–29%) | In 1 condition |
| PLA2G6phospholipase A2 group VI | Sometimes (5–29%) | In 1 condition |
| RARS1arginyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TBL1XR1TBL1X/Y related 1 | Sometimes (5–29%) | In 2 conditions |
| TMEM106Btransmembrane protein 106B | Sometimes (5–29%) | In 1 condition |
| AIPL1AIP like 1 HSP90 co-chaperone | Not recorded | In 1 condition |
| ATOH7atonal bHLH transcription factor 7 | Not recorded | In 1 condition |
| CRXcone-rod homeobox | Not recorded | In 1 condition |
| FRMD7FERM domain containing 7 | Not recorded | In 1 condition |
| NUP62nucleoporin 62 | Not recorded | In 1 condition |
| OPN1LWopsin 1, long wave sensitive | Not recorded | In 1 condition |
| OPN1MWopsin 1, medium wave sensitive | Not recorded | In 1 condition |
| RPGRIP1RPGR interacting protein 1 | Not recorded | In 1 condition |
| TENM3teneurin transmembrane protein 3 | 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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