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Trait
Squamous cell carcinoma
The presence of squamous cell carcinoma of the skin.
Summary
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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/squamous-cell-carcinoma.json"
page <- fromJSON(url)
page$trait$nameSquamous cell carcinomaHP:0002860
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Get my Genome Test51 genes linked to Squamous cell carcinoma
Changes in these genes cause rare conditions in which Squamous cell carcinoma 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 |
|---|---|---|
| GJB2gap junction protein beta 2 | Always | In 3 conditions |
| SASH1SAM and SH3 domain containing 1 | Always | In 1 condition |
| BRD4bromodomain containing 4 | Often (30–79%) | In 1 condition |
| CIB1calcium and integrin binding 1 | Often (30–79%) | In 2 conditions |
| COL7A1collagen type VII alpha 1 chain | Often (30–79%) | In 6 conditions |
| MMP1matrix metallopeptidase 1 | Often (30–79%) | In 1 condition |
| NUTM1NUT midline carcinoma family member 1 | Often (30–79%) | In 1 condition |
| POLHDNA polymerase eta | Often (30–79%) | In 2 conditions |
| AARS1alanyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| BLMBLM RecQ like helicase | Sometimes (5–29%) | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| CTSCcathepsin C | Sometimes (5–29%) | In 1 condition |
| DBR1debranching RNA lariats 1 | Sometimes (5–29%) | In 1 condition |
| DOCK8dedicator of cytokinesis 8 | Sometimes (5–29%) | In 2 conditions |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 2 conditions |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| FDPSfarnesyl diphosphate synthase | Sometimes (5–29%) | In 1 condition |
| FERMT1FERM domain containing kindlin 1 | Sometimes (5–29%) | In 1 condition |
| GTF2E2general transcription factor IIE subunit 2 | Sometimes (5–29%) | In 1 condition |
| GTF2H5general transcription factor IIH subunit 5 | Sometimes (5–29%) | In 1 condition |
| IL7interleukin 7 | Sometimes (5–29%) | In 1 condition |
| LAMA3laminin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| MPLKIPM-phase specific PLK1 interacting protein | Sometimes (5–29%) | In 1 condition |
| MVDmevalonate diphosphate decarboxylase | Sometimes (5–29%) | In 1 condition |
| MVKmevalonate kinase | Sometimes (5–29%) | In 1 condition |
| NTHL1nth like DNA glycosylase 1 | Sometimes (5–29%) | In 1 condition |
| RECQL4RecQ like helicase 4 | Sometimes (5–29%) | In 2 conditions |
| RNF113Aring finger protein 113A | Sometimes (5–29%) | In 1 condition |
| SLC17A9solute carrier family 17 member 9 | Sometimes (5–29%) | In 1 condition |
| SLX4SLX4 structure-specific endonuclease subunit | Sometimes (5–29%) | In 1 condition |
| TARS1threonyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TMC6transmembrane channel like 6 | Sometimes (5–29%) | In 1 condition |
| TMC8transmembrane channel like 8 | Sometimes (5–29%) | In 1 condition |
| WNT10AWnt family member 10A | Sometimes (5–29%) | In 2 conditions |
| WRNWRN RecQ like helicase | Sometimes (5–29%) | In 1 condition |
| AAGABalpha and gamma adaptin binding protein | Rarely (1–4%) | In 1 condition |
| ANAPC1anaphase promoting complex subunit 1 | Rarely (1–4%) | In 1 condition |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| COL14A1collagen type XIV alpha 1 chain | Rarely (1–4%) | In 1 condition |
| GATA1GATA binding protein 1 | Rarely (1–4%) | In 1 condition |
| GJB6gap junction protein beta 6 | Rarely (1–4%) | In 1 condition |
| UROSuroporphyrinogen III synthase | Rarely (1–4%) | In 1 condition |
| CDKN2Acyclin dependent kinase inhibitor 2A | Not recorded | In 1 condition |
| COL17A1collagen type XVII alpha 1 chain | Not recorded | In 1 condition |
| DKC1dyskerin pseudouridine synthase 1 | Not recorded | In 1 condition |
| ING1inhibitor of growth family member 1 | Not recorded | In 1 condition |
| NLRP1NLR family pyrin domain containing 1 | Not recorded | In 1 condition |
| PSENENpresenilin enhancer, gamma-secretase subunit | Not recorded | In 1 condition |
| TNFRSF10BTNF receptor superfamily member 10b | 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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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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