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Traits
Traits linked to AGO1
argonaute RISC component 1
The Human Phenotype Ontology links 35 traits to AGO1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Delayed ability to walk | Always |
| Delayed speech and language development | Always |
| Febrile seizure (within the age range of 3 months to 6 years) | Always |
| Focal impaired awareness seizure | Always |
| Global developmental delay | Always |
| Globus pallidus calcification | Always |
| Grand mal seizures | Always |
| Intellectual disability | Always |
| IQ between 34 and 49 | Always |
| More active than typical | Always |
| Repeated seizures without recovery between them | Always |
| Repetitive movements | Always |
| Anxiety | Very often (80–99%) |
| Autism spectrum disorder | Very often (80–99%) |
| Motor delay | Very often (80–99%) |
| Aggressive behavior | Often (30–79%) |
| Attention deficit | Often (30–79%) |
| Difficulty sleeping | Often (30–79%) |
| Epilepsy | Often (30–79%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Bulbous nose | Always |
| Corners of eye widely separated | Always |
| Downward slanting of the opening between the eyelids | Always |
| Eye folds | Always |
| Round face | Always |
| Wide nasal bridge | Always |
| Almond shaped eyes | Not recorded |
| High forehead | Not recorded |
| Short nose | Not recorded |
| Thin red part of the upper lip | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties | Often (30–79%) |
| Acid reflux | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Large ears | Always |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Cross-eyed | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Mild short stature | 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 AGO1 and how often each is seen. Find out more at hpo.jax.org.
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