Trait
Born with teeth
Clinical name: Natal tooth
A tooth present at birth or erupting within the first month of life.
Summary
- Also called
- Teeth present at birth, Natal teeth, Neonatal teeth
- Body system
- Abnormality of head or neck
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test39 genes linked to Born with teeth
Changes in these genes cause rare conditions in which Born with teeth 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 |
|---|---|---|
| BCL11BBCL11 transcription factor B | Always | In 1 condition |
| DSPdesmoplakin | Always | In 2 conditions |
| FGFR2fibroblast growth factor receptor 2 | Always | In 3 conditions |
| GTF2H5general transcription factor IIH subunit 5 | Always | In 1 condition |
| POLR3ARNA polymerase III subunit A | Always | In 2 conditions |
| SUPT7LSPT7 like, STAGA complex subunit gamma | Always | In 1 condition |
| FLNAfilamin A | Very often (80–99%) | In 1 condition |
| CHD6chromodomain helicase DNA binding protein 6 | Often (30–79%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Often (30–79%) | In 2 conditions |
| INTUinturned planar cell polarity protein | Often (30–79%) | In 1 condition |
| JUPjunction plakoglobin | Often (30–79%) | In 1 condition |
| POLR3BRNA polymerase III subunit B | Often (30–79%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Often (30–79%) | In 1 condition |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Often (30–79%) | In 1 condition |
| VARS1valyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| DPH1diphthamide biosynthesis 1 | Sometimes (5–29%) | In 1 condition |
| EHMT1euchromatic histone lysine methyltransferase 1 | Sometimes (5–29%) | In 2 conditions |
| FAM20CFAM20C golgi associated secretory pathway kinase | Sometimes (5–29%) | In 1 condition |
| KDF1keratinocyte differentiation factor 1 | Sometimes (5–29%) | In 1 condition |
| KDM6Alysine demethylase 6A | Sometimes (5–29%) | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Sometimes (5–29%) | In 1 condition |
| KRT16keratin 16 | Sometimes (5–29%) | In 1 condition |
| KRT17keratin 17 | Sometimes (5–29%) | In 2 conditions |
| KRT6Akeratin 6A | Sometimes (5–29%) | In 1 condition |
| KRT6Bkeratin 6B | Sometimes (5–29%) | In 2 conditions |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | Sometimes (5–29%) | In 2 conditions |
| CREBBPCREB binding lysine acetyltransferase | Rarely (1–4%) | In 2 conditions |
| EP300EP300 lysine acetyltransferase | Rarely (1–4%) | In 1 condition |
| KMT2Clysine methyltransferase 2C | Rarely (1–4%) | In 1 condition |
| MID1midline 1 | Rarely (1–4%) | In 1 condition |
| NEK1NIMA related kinase 1 | Rarely (1–4%) | In 1 condition |
| AMER1APC membrane recruitment protein 1 | Not recorded | In 1 condition |
| C2CD3C2 domain containing 3 centriole elongation regulator | Not recorded | In 1 condition |
| CEP120centrosomal protein 120 | Not recorded | In 1 condition |
| CILK1ciliogenesis associated kinase 1 | Not recorded | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Not recorded | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Not recorded | In 1 condition |
| MKS1MKS transition zone complex subunit 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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