Traits

Traits linked to SLC41A1

solute carrier family 41 member 1

The Human Phenotype Ontology links 12 traits to SLC41A1, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the genitourinary system

Trait	How often it is seen
Increased urine output	Always
Periglomerular fibrosis	Always
Stage 5 chronic kidney disease	Always
Tubular luminal dilatation	Always
Renal failure	Often (30–79%)

Abnormality of the respiratory system

Trait	How often it is seen
Cough	Always
Lung infiltrates	Always
Permanent enlargement of the airways of the lungs	Often (30–79%)

Laboratory abnormality

Trait	How often it is seen
Elevated creatinine	Always
Episodic fever	Always

Abnormality of the immune system

Trait	How often it is seen
Recurrent respiratory infections	Always

Abnormality of the nervous system

Trait	How often it is seen
Extreme thirst	Always

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 SLC41A1 and how often each is seen. Find out more at hpo.jax.org.

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