Trait
Skin writing
Clinical name: Dermatographic urticaria
An exaggerated whealing tendency when the skin is stroked, that is, formation of red, itchy bumps and lines on the skin as a result of pressure on the skin (for instance, stroking the skin with a pen or tongue depressor).
Summary
- Also called
- Dermatographism, Dermographism
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/dermatographic-urticaria.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Skin writing, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Skin writing
Changes in these genes cause rare conditions in which Skin writing 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 |
|---|---|---|
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| IL12Ainterleukin 12A | Very often (80–99%) | In 1 condition |
| IL12RB1interleukin 12 receptor subunit beta 1 | Very often (80–99%) | In 1 condition |
| IRF5interferon regulatory factor 5 | Very often (80–99%) | In 1 condition |
| MMEL1membrane metalloendopeptidase like 1 | Very often (80–99%) | In 1 condition |
| POU2AF1POU class 2 homeobox associating factor 1 | Very often (80–99%) | In 1 condition |
| SERPING1serpin family G member 1 | Very often (80–99%) | In 1 condition |
| SPIBSpi-B transcription factor | Very often (80–99%) | In 1 condition |
| TNFSF15TNF superfamily member 15 | Very often (80–99%) | In 1 condition |
| TNPO3transportin 3 | Very often (80–99%) | In 1 condition |
| PLCG2phospholipase C gamma 2 | Sometimes (5–29%) | In 1 condition |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Sometimes (5–29%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Rarely (1–4%) | In 1 condition |
| SLC27A4solute carrier family 27 member 4 | 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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