Trait
Papillary thyroid carcinoma
The presence of a papillary adenocarcinoma of the thyroid gland.
Summary
- Also called
- Papillary carcinoma of thyroid, Thyroid papillary carcinoma
Reference genomeGRCh38hg38
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Get my Genome Test24 genes linked to Papillary thyroid carcinoma
Changes in these genes cause rare conditions in which Papillary 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 |
|---|---|---|
| SEC23BSEC23 homolog B, COPII component | Very often (80–99%) | In 1 condition |
| FOXE1forkhead box E1 | Often (30–79%) | In 2 conditions |
| APCAPC regulator of Wnt signaling pathway | Sometimes (5–29%) | In 3 conditions |
| HABP2hyaluronan binding protein 2 | Sometimes (5–29%) | In 1 condition |
| MINPP1multiple inositol-polyphosphate phosphatase 1 | Sometimes (5–29%) | In 2 conditions |
| ARID1AAT-rich interaction domain 1A | Rarely (1–4%) | In 1 condition |
| ARID1BAT-rich interaction domain 1B | Rarely (1–4%) | In 1 condition |
| ARID2AT-rich interaction domain 2 | Rarely (1–4%) | In 1 condition |
| DPF2double PHD fingers 2 | 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 1 condition |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Rarely (1–4%) | In 1 condition |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Rarely (1–4%) | In 1 condition |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Rarely (1–4%) | In 1 condition |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Rarely (1–4%) | In 1 condition |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Rarely (1–4%) | In 1 condition |
| SOX11SRY-box transcription factor 11 | Rarely (1–4%) | In 1 condition |
| SOX4SRY-box transcription factor 4 | Rarely (1–4%) | In 1 condition |
| DICER1dicer 1, ribonuclease III | Not recorded | In 1 condition |
| HRASHRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| JAG1jagged canonical Notch ligand 1 | Not recorded | In 1 condition |
| NKX2-1NK2 homeobox 1 | Not recorded | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Not recorded | In 1 condition |
| SRGAP1SLIT-ROBO Rho GTPase activating protein 1 | 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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