Trait
Thyroid carcinoma
The presence of a carcinoma of the thyroid gland.
Summary
Reference genomeGRCh38hg38
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Get my Genome Test25 genes linked to Thyroid carcinoma
Changes in these genes cause rare conditions in which Thyroid 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 |
|---|---|---|
| AKT1AKT serine/threonine kinase 1 | Often (30–79%) | In 1 condition |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Sometimes (5–29%) | In 1 condition |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Sometimes (5–29%) | In 1 condition |
| FOXI1forkhead box I1 | Sometimes (5–29%) | In 2 conditions |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Sometimes (5–29%) | In 2 conditions |
| MEN1menin 1 | Sometimes (5–29%) | In 1 condition |
| PTENphosphatase and tensin homolog | Sometimes (5–29%) | In 2 conditions |
| SLC26A4solute carrier family 26 member 4 | Sometimes (5–29%) | In 2 conditions |
| WRNWRN RecQ like helicase | Sometimes (5–29%) | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Rarely (1–4%) | In 1 condition |
| CASP10caspase 10 | Rarely (1–4%) | In 1 condition |
| CDC73cell division cycle 73 | Rarely (1–4%) | In 2 conditions |
| CDKN2Acyclin dependent kinase inhibitor 2A | Rarely (1–4%) | In 1 condition |
| CHEK2checkpoint kinase 2 | Rarely (1–4%) | In 1 condition |
| DICER1dicer 1, ribonuclease III | Rarely (1–4%) | In 1 condition |
| FASFas cell surface death receptor | Rarely (1–4%) | In 1 condition |
| FASLGFas ligand | Rarely (1–4%) | In 1 condition |
| GREM1gremlin 1, DAN family BMP antagonist | Rarely (1–4%) | In 1 condition |
| HEPACAMhepatic and glial cell adhesion molecule | Rarely (1–4%) | In 1 condition |
| KEAP1kelch like ECH associated protein 1 | Rarely (1–4%) | In 1 condition |
| MDM2MDM2 proto-oncogene | Rarely (1–4%) | In 1 condition |
| PDE11Aphosphodiesterase 11A | Rarely (1–4%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Rarely (1–4%) | In 2 conditions |
| TP53tumor protein p53 | Rarely (1–4%) | In 1 condition |
| TGthyroglobulin | 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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