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Traits

Traits linked to TMEM185A

transmembrane protein 185A

The Human Phenotype Ontology links 2 traits to TMEM185A, by body system: features seen in people with one of the gene's rare conditions.

Abnormal cellular phenotype

TraitHow often it is seen
Folate-dependent fragile site at Xq28Very often (80–99%)

Abnormality of the nervous system

TraitHow often it is seen
Neurodevelopmental delaySometimes (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 TMEM185A and how often each is seen. Find out more at hpo.jax.org.

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