Trait
Reticular hyperpigmentation
Increased pigmentation of the skin with a netlike (reticular) pattern.
Summary
- Also called
- Reticulate hyperpigmentation
- Body system
- Abnormality of the integument
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test13 genes linked to Reticular hyperpigmentation
Changes in these genes cause rare conditions in which Reticular hyperpigmentation 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 |
|---|---|---|
| MPV17mitochondrial inner membrane protein MPV17 | Always | In 1 condition |
| NHP2NHP2 ribonucleoprotein | Always | In 1 condition |
| NOP10NOP10 ribonucleoprotein | Always | In 1 condition |
| POLA1DNA polymerase alpha 1, catalytic subunit | Always | In 1 condition |
| TP53tumor protein p53 | Always | In 1 condition |
| TERCtelomerase RNA component | Very often (80–99%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Very often (80–99%) | In 1 condition |
| TINF2TERF1 interacting nuclear factor 2 | Very often (80–99%) | In 1 condition |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Often (30–79%) | In 1 condition |
| RPA1replication protein A1 | Sometimes (5–29%) | In 1 condition |
| KRT14keratin 14 | Not recorded | In 2 conditions |
| POFUT1protein O-fucosyltransferase 1 | Not recorded | In 1 condition |
| PORCNporcupine O-acyltransferase | 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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