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Traits
Traits linked to GATC
glutamyl-tRNA amidotransferase subunit C
The Human Phenotype Ontology links 14 traits to GATC, by body system: features seen in people with one of the gene's rare conditions.
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Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Increased lactate in body | Always |
| Elevated blood creatine phosphokinase | Often (30–79%) |
| Nonimmune hydrops fetalis | Often (30–79%) |
| Low blood sugar | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Decreased activity of mitochondrial complex I | Not recorded |
| Decreased activity of mitochondrial complex III | Not recorded |
| Decreased activity of mitochondrial complex IV | Not recorded |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Low number of red blood cells or hemoglobin | Always |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Premature birth | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Disease of the heart muscle | Always |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Decreased liver function | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Hearing impairment | Always |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Low blood cortisol level | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Prenatal growth deficiency | 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 GATC and how often each is seen. Find out more at hpo.jax.org.
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