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Trait
Slow pupillary light response
Reduced velocity and acceleration in the pupillary light response.
Summary
- Also called
- Sluggish pupillary reaction, Sluggish pupillary reactions to light
- Body system
- Abnormality of the eye
Slow pupillary light responseHP:0030211
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Read the genes linked to Slow pupillary light response, and the rest of your genome, with one test.
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Get my Genome Test46 genes linked to Slow pupillary light response
Changes in these genes cause rare conditions in which Slow pupillary light response 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 |
|---|---|---|
| CHRM3cholinergic receptor muscarinic 3 | Always | In 1 condition |
| FDXRferredoxin reductase | Always | In 1 condition |
| KLC4kinesin light chain 4 | Always | In 1 condition |
| RPGRIP1RPGR interacting protein 1 | Always | In 2 conditions |
| TULP1TUB like protein 1 | Always | In 2 conditions |
| CHRNA3cholinergic receptor nicotinic alpha 3 subunit | Very often (80–99%) | In 1 condition |
| COL25A1collagen type XXV alpha 1 chain | Very often (80–99%) | In 1 condition |
| KIF21Akinesin family member 21A | Very often (80–99%) | In 1 condition |
| PHOX2Apaired like homeobox 2A | Very often (80–99%) | In 1 condition |
| TUBA1Atubulin alpha 1a | Very often (80–99%) | In 1 condition |
| TUBB2Btubulin beta 2B class IIb | Very often (80–99%) | In 1 condition |
| TUBB3tubulin beta 3 class III | Very often (80–99%) | In 1 condition |
| AIMP1aminoacyl tRNA synthetase complex interacting multifunctional protein 1 | Often (30–79%) | In 1 condition |
| AIPL1AIP like 1 HSP90 co-chaperone | Often (30–79%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Often (30–79%) | In 1 condition |
| CABP4calcium binding protein 4 | Often (30–79%) | In 1 condition |
| CEP290centrosomal protein 290 | Often (30–79%) | In 1 condition |
| CRB1crumbs cell polarity complex component 1 | Often (30–79%) | In 1 condition |
| CRXcone-rod homeobox | Often (30–79%) | In 1 condition |
| GDF6growth differentiation factor 6 | Often (30–79%) | In 1 condition |
| GUCY2Dguanylate cyclase 2D, retinal | Often (30–79%) | In 1 condition |
| IFT140intraflagellar transport 140 | Often (30–79%) | In 1 condition |
| IMPDH1inosine monophosphate dehydrogenase 1 | Often (30–79%) | In 1 condition |
| IQCB1IQ motif containing B1 | Often (30–79%) | In 1 condition |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Often (30–79%) | In 1 condition |
| LCA5lebercilin LCA5 | Often (30–79%) | In 1 condition |
| LRATlecithin retinol acyltransferase | Often (30–79%) | In 1 condition |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Often (30–79%) | In 1 condition |
| OTX2orthodenticle homeobox 2 | Often (30–79%) | In 1 condition |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Often (30–79%) | In 1 condition |
| PMP22peripheral myelin protein 22 | Often (30–79%) | In 1 condition |
| PRPH2peripherin 2 | Often (30–79%) | In 1 condition |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Often (30–79%) | In 1 condition |
| RD3RD3 regulator of GUCY2D | Often (30–79%) | In 1 condition |
| RDH12retinol dehydrogenase 12 | Often (30–79%) | In 1 condition |
| RPE65retinoid isomerohydrolase RPE65 | Often (30–79%) | In 1 condition |
| SPATA7spermatogenesis associated 7 | Often (30–79%) | In 1 condition |
| TUBB4Btubulin beta 4B class IVb | Often (30–79%) | In 1 condition |
| USP45ubiquitin specific peptidase 45 | Often (30–79%) | In 1 condition |
| COL13A1collagen type XIII alpha 1 chain | Sometimes (5–29%) | In 1 condition |
Show 6 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Sometimes (5–29%) | In 1 condition |
| GALCgalactosylceramidase | Sometimes (5–29%) | In 1 condition |
| LAMB2laminin subunit beta 2 | Sometimes (5–29%) | In 1 condition |
| PSAPprosaposin | Sometimes (5–29%) | In 1 condition |
| COL18A1collagen type XVIII alpha 1 chain | Not recorded | In 1 condition |
| MPZmyelin protein zero | 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.
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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