Trait
Taurodontia
Increased volume of dental pulp of permanent molar characterized by a crown body-root ratio equal or larger than 1:1 or an elongated pulp chambers and apical displacement of the bifurcation or trifurcation of the roots.
Summary
- Also called
- Taurodont, Taurodontism
- 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 Test55 genes linked to Taurodontia
Changes in these genes cause rare conditions in which Taurodontia 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 |
|---|---|---|
| BRF1BRF1 general transcription factor IIIB subunit | Always | In 2 conditions |
| LEF1lymphoid enhancer binding factor 1 | Always | In 1 condition |
| SMOC2SPARC related modular calcium binding 2 | Always | In 1 condition |
| TP63tumor protein p63 | Always | In 2 conditions |
| KCTD1potassium channel tetramerization domain containing 1 | Very often (80–99%) | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Very often (80–99%) | In 1 condition |
| PEX6peroxisomal biogenesis factor 6 | Very often (80–99%) | In 1 condition |
| RAI1retinoic acid induced 1 | Very often (80–99%) | In 1 condition |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Often (30–79%) | In 1 condition |
| CPLX1complexin 1 | Often (30–79%) | In 1 condition |
| CTBP1C-terminal binding protein 1 | Often (30–79%) | In 1 condition |
| CTC1CST telomere replication complex component 1 | Often (30–79%) | In 1 condition |
| DKC1dyskerin pseudouridine synthase 1 | Often (30–79%) | In 1 condition |
| DLX3distal-less homeobox 3 | Often (30–79%) | In 3 conditions |
| FGF3fibroblast growth factor 3 | Often (30–79%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Often (30–79%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Often (30–79%) | In 1 condition |
| NELFAnegative elongation factor complex member A | Often (30–79%) | In 1 condition |
| NHP2NHP2 ribonucleoprotein | Often (30–79%) | In 1 condition |
| NOP10NOP10 ribonucleoprotein | Often (30–79%) | In 1 condition |
| NPM1nucleophosmin 1 | Often (30–79%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Often (30–79%) | In 1 condition |
| PARNpoly(A)-specific ribonuclease | Often (30–79%) | In 1 condition |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Often (30–79%) | In 1 condition |
| RTEL1regulator of telomere elongation helicase 1 | Often (30–79%) | In 1 condition |
| TERCtelomerase RNA component | Often (30–79%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Often (30–79%) | In 1 condition |
| TINF2TERF1 interacting nuclear factor 2 | Often (30–79%) | In 1 condition |
| TYMSthymidylate synthetase | Often (30–79%) | In 1 condition |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Often (30–79%) | In 1 condition |
| WDR19WD repeat domain 19 | Often (30–79%) | In 2 conditions |
| WRAP53WD repeat containing antisense to TP53 | Often (30–79%) | In 1 condition |
| C1Rcomplement C1r | Sometimes (5–29%) | In 1 condition |
| C1Scomplement C1s | Sometimes (5–29%) | In 1 condition |
| EDAectodysplasin A | Sometimes (5–29%) | In 2 conditions |
| EDARADDEDAR associated via death domain | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Sometimes (5–29%) | In 2 conditions |
| GREM2gremlin 2, DAN family BMP antagonist | Sometimes (5–29%) | In 2 conditions |
| IFT122intraflagellar transport 122 | Sometimes (5–29%) | In 1 condition |
Show 15 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| IFT43intraflagellar transport 43 | Sometimes (5–29%) | In 1 condition |
| IFT52intraflagellar transport 52 | Sometimes (5–29%) | In 1 condition |
| IRF6interferon regulatory factor 6 | Sometimes (5–29%) | In 1 condition |
| LRP6LDL receptor related protein 6 | Sometimes (5–29%) | In 2 conditions |
| MSX1msh homeobox 1 | Sometimes (5–29%) | In 1 condition |
| NEK1NIMA related kinase 1 | Sometimes (5–29%) | In 1 condition |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Sometimes (5–29%) | In 1 condition |
| PAX9paired box 9 | Sometimes (5–29%) | In 1 condition |
| SUMO1small ubiquitin like modifier 1 | Sometimes (5–29%) | In 1 condition |
| TGFAtransforming growth factor alpha | Sometimes (5–29%) | In 1 condition |
| WDR35WD repeat domain 35 | Sometimes (5–29%) | In 1 condition |
| WNT10AWnt family member 10A | Sometimes (5–29%) | In 1 condition |
| WNT10BWnt family member 10B | Sometimes (5–29%) | In 1 condition |
| CHD3chromodomain helicase DNA binding protein 3 | Rarely (1–4%) | In 1 condition |
| GALNT3polypeptide N-acetylgalactosaminyltransferase 3 | 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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