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Traits
Traits linked to DRG1
developmentally regulated GTP binding protein 1
The Human Phenotype Ontology links 25 traits to DRG1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormally small head | Always |
| Broad head shape | Always |
| Flattened bony protrusion above eyes | Always |
| Prominent forehead | Always |
| Short opening between the eyelids | Always |
| Wide nasal bridge | Always |
| Widely spaced teeth | Always |
| Drooping lower lip | Often (30–79%) |
| Short eyelashes | Often (30–79%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Neurodevelopmental delay | Always |
| Epilepsy | Sometimes (5–29%) |
| Myelomeningocele | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Always |
| Prenatal growth deficiency | Always |
| Proportionate short stature | Always |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Always |
| Ears rotated toward back of head | Often (30–79%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Eczema | Always |
| Recurrent infections | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Permanent flexion of the finger or toe | Always |
| Involuntary muscle stiffness, contraction, or spasm | Often (30–79%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Increased antibody level in blood | Often (30–79%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Autoimmune hemolytic anemia | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Club feet | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Dry skin | Often (30–79%) |
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 DRG1 and how often each is seen. Find out more at hpo.jax.org.
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