Trait
Prominent eyelashes
Eyelashes that draw the attention of the viewer due to increased density and/or length and/or curl without meeting the criteria of trichomegaly.
Summary
- Also called
- Thick eyelashes
This 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/prominent-eyelashes.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Prominent eyelashes, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test19 genes linked to Prominent eyelashes
Changes in these genes cause rare conditions in which Prominent eyelashes 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 |
|---|---|---|
| KDM6Blysine demethylase 6B | Always | In 1 condition |
| VPS13Bvacuolar protein sorting 13 homolog B | Always | In 1 condition |
| ARID1AAT-rich interaction domain 1A | Very often (80–99%) | In 1 condition |
| ARID1BAT-rich interaction domain 1B | Very often (80–99%) | In 1 condition |
| ARID2AT-rich interaction domain 2 | Very often (80–99%) | In 1 condition |
| DPF2double PHD fingers 2 | Very often (80–99%) | In 1 condition |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Very often (80–99%) | In 1 condition |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Very often (80–99%) | In 1 condition |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Very often (80–99%) | In 1 condition |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Very often (80–99%) | In 1 condition |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Very often (80–99%) | In 1 condition |
| SOX11SRY-box transcription factor 11 | Very often (80–99%) | In 1 condition |
| SOX4SRY-box transcription factor 4 | Very often (80–99%) | In 1 condition |
| PYCR2pyrroline-5-carboxylate reductase 2 | Often (30–79%) | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Often (30–79%) | In 2 conditions |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| KDM6Alysine demethylase 6A | Not recorded | In 1 condition |
| KMT2Dlysine methyltransferase 2D | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks