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Traits

Traits linked to SLC36A2

solute carrier family 36 member 2

The Human Phenotype Ontology links 9 traits to SLC36A2, by body system: features seen in people with one of the gene's rare conditions.

Laboratory abnormality

TraitHow often it is seen
Elevated urinary hydroxyprolineAlways
High urine glycine levelsAlways
ProlinuriaAlways
Elevated blood glycine levelsNot recorded
High blood hydroxyproline levelsNot recorded
HyperprolinemiaNot recorded

Abnormality of the eye

TraitHow often it is seen
Abnormality of the eyeNot recorded

Abnormality of the genitourinary system

TraitHow often it is seen
Calcium oxalate nephrolithiasisNot recorded

Abnormality of the nervous system

TraitHow often it is seen
Intellectual disabilityNot recorded

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 SLC36A2 and how often each is seen. Find out more at hpo.jax.org.

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