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Traits
Traits linked to SLC2A3
solute carrier family 2 member 3
The Human Phenotype Ontology links 52 traits to SLC2A3, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the nervous system
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormality of eye movement | Often (30–79%) |
| Staring gaze | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Generalized muscle weakness | Often (30–79%) |
| Rigidity | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Weight loss | Often (30–79%) |
| Decreased body mass index | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormality of the sense of smell | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Oral-pharyngeal dysphagia | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormal libido | Often (30–79%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Abnormality of cholesterol metabolism | 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 SLC2A3 and how often each is seen. Find out more at hpo.jax.org.
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