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Traits
Traits linked to SUMO1
small ubiquitin like modifier 1
The Human Phenotype Ontology links 25 traits to SUMO1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Failure of development of more than six teeth | Always |
| One sided cleft palate | Always |
| One sided cleft upper lip | Always |
| Chewing difficulties | Very often (80–99%) |
| Absence of premolar | Often (30–79%) |
| Absence of six year molar | Often (30–79%) |
| Absence of upper lateral incisor | Often (30–79%) |
| Absent central incisor | Often (30–79%) |
| Bad bite | Often (30–79%) |
| Decreased length of dental roots | Often (30–79%) |
| Decreased size of tooth | Often (30–79%) |
| Delayed eruption of permanent teeth | Often (30–79%) |
| Delayed eruption of teeth | Often (30–79%) |
| Widely spaced teeth | Often (30–79%) |
| Abnormality of canine | Sometimes (5–29%) |
| Abnormality of dental shape | Sometimes (5–29%) |
| Abnormality of shape of baby molar | Sometimes (5–29%) |
| Absence of lower premolar | Sometimes (5–29%) |
| Cleft of the mouth | Sometimes (5–29%) |
| Decreased size of teeth | Sometimes (5–29%) |
| Outward turned lips | Sometimes (5–29%) |
| Peg-shaped maxillary lateral incisors | Sometimes (5–29%) |
| Short face | Sometimes (5–29%) |
| Taurodontia | Sometimes (5–29%) |
| Thin dental enamel | Sometimes (5–29%) |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to SUMO1 and how often each is seen. Find out more at hpo.jax.org.
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