Trait
Warts
Clinical name: Verrucae
Warts, benign growths on the skin or mucous membranes that cause cosmetic problems as well as pain and discomfort. Warts most often occur on the hands, feet, and genital areas.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test31 genes linked to Warts
Changes in these genes cause rare conditions in which Warts 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 |
|---|---|---|
| CD28CD28 molecule | Always | In 1 condition |
| CIB1calcium and integrin binding 1 | Always | In 2 conditions |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| PDCD1programmed cell death 1 | Always | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Always | In 1 condition |
| SEC61A1SEC61 translocon subunit alpha 1 | Always | In 1 condition |
| STK4serine/threonine kinase 4 | Always | In 1 condition |
| DOCK8dedicator of cytokinesis 8 | Very often (80–99%) | In 1 condition |
| IL7interleukin 7 | Very often (80–99%) | In 2 conditions |
| TMC6transmembrane channel like 6 | Very often (80–99%) | In 2 conditions |
| TMC8transmembrane channel like 8 | Very often (80–99%) | In 1 condition |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Often (30–79%) | In 1 condition |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Often (30–79%) | In 1 condition |
| CXCR4C-X-C motif chemokine receptor 4 | Often (30–79%) | In 2 conditions |
| DCLRE1CDNA cross-link repair 1C | Often (30–79%) | In 1 condition |
| ECM1extracellular matrix protein 1 | Often (30–79%) | In 1 condition |
| RNF31ring finger protein 31 | Often (30–79%) | In 1 condition |
| SASH3SAM and SH3 domain containing 3 | Often (30–79%) | In 1 condition |
| BLNKB cell linker | Sometimes (5–29%) | In 1 condition |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| GATA2GATA binding protein 2 | Sometimes (5–29%) | In 1 condition |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 1 condition |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 2 conditions |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 1 condition |
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| FCN3ficolin 3 | Not recorded | In 1 condition |
| IVNS1ABPinfluenza virus NS1A binding protein | 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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