Trait
Dentinogenesis imperfecta
Developmental dysplasia of dentin.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Dentinogenesis imperfecta, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Dentinogenesis imperfecta
Changes in these genes cause rare conditions in which Dentinogenesis imperfecta 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 |
|---|---|---|
| MIA3MIA SH3 domain ER export factor 3 | Always | In 1 condition |
| SERPINH1serpin family H member 1 | Always | In 1 condition |
| PPIBpeptidylprolyl isomerase B | Very often (80–99%) | In 1 condition |
| TRIP11thyroid hormone receptor interactor 11 | Very often (80–99%) | In 2 conditions |
| P4HBprolyl 4-hydroxylase subunit beta | Often (30–79%) | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Often (30–79%) | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Sometimes (5–29%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Sometimes (5–29%) | In 4 conditions |
| COL1A2collagen type I alpha 2 chain | Sometimes (5–29%) | In 3 conditions |
| FKBP10FKBP prolyl isomerase 10 | Sometimes (5–29%) | In 1 condition |
| DSPPdentin sialophosphoprotein | Not recorded | In 3 conditions |
| SEC24DSEC24 homolog D, COPII component | Not recorded | In 1 condition |
| ZNF469zinc finger protein 469 | 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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