Trait
Cone shaped tooth
Clinical name: Conical tooth
An abnormal conical form of the teeth, that is, a tooth whose sides converge or taper together incisally.
Summary
- Also called
- Peg shaped tooth, Pointed tooth, Conoid tooth, Peg shaped teeth, Peg tooth, Peg-shaped teeth, Peg-shaped tooth
- 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 Test29 genes linked to Cone shaped tooth
Changes in these genes cause rare conditions in which Cone shaped tooth 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 |
|---|---|---|
| CTNND1catenin delta 1 | Always | In 2 conditions |
| EDARectodysplasin A receptor | Always | In 1 condition |
| EDARADDEDAR associated via death domain | Always | In 2 conditions |
| FGFR3fibroblast growth factor receptor 3 | Always | In 1 condition |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Always | In 6 conditions |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| NFKBIANFKB inhibitor alpha | Always | In 2 conditions |
| RNU6ATACRNA, U6atac small nuclear | Always | In 1 condition |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | Always | In 1 condition |
| TSPEARthrombospondin type laminin G domain and EAR repeats | Always | In 1 condition |
| CTNNB1catenin beta 1 | Very often (80–99%) | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Very often (80–99%) | In 2 conditions |
| EVC2EvC ciliary complex subunit 2 | Very often (80–99%) | In 2 conditions |
| FGF3fibroblast growth factor 3 | Very often (80–99%) | In 2 conditions |
| MSX1msh homeobox 1 | Very often (80–99%) | In 1 condition |
| ALX4ALX homeobox 4 | Often (30–79%) | In 2 conditions |
| CDH1cadherin 1 | Often (30–79%) | In 2 conditions |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Often (30–79%) | In 1 condition |
| RHOAras homolog family member A | Often (30–79%) | In 1 condition |
| RUSC2RUN and SH3 domain containing 2 | Often (30–79%) | In 1 condition |
| ANAPC1anaphase promoting complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| ARID1BAT-rich interaction domain 1B | Sometimes (5–29%) | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Sometimes (5–29%) | In 1 condition |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Sometimes (5–29%) | In 1 condition |
| DHODHdihydroorotate dehydrogenase (quinone) | Not recorded | In 1 condition |
| EDAectodysplasin A | Not recorded | In 1 condition |
| NECTIN4nectin cell adhesion molecule 4 | Not recorded | In 1 condition |
| SATB2SATB homeobox 2 | Not recorded | In 1 condition |
| TP63tumor protein p63 | Not recorded | In 2 conditions |
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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