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Traits
Traits linked to PRKCG
protein kinase C gamma
The Human Phenotype Ontology links 27 traits to PRKCG, 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 |
|---|---|
| Inability to coordinate movements when walking | Very often (80–99%) |
| Cerebellar vermis atrophy | Often (30–79%) |
| Limb ataxia | Often (30–79%) |
| Progressive cerebellar ataxia | Often (30–79%) |
| Cognitive impairment | Sometimes (5–29%) |
| Difficulty articulating speech | Sometimes (5–29%) |
| Jerking | Sometimes (5–29%) |
| Somatic sensory dysfunction | Sometimes (5–29%) |
| Tremor | Sometimes (5–29%) |
| Attention deficit | Not recorded |
| Degeneration of cerebellum | Not recorded |
| Depression | Not recorded |
| Focal dystonia | Not recorded |
| Impaired vibration sensation at ankles | Not recorded |
| Increased reflexes | Not recorded |
| Lack of coordination of movement | Not recorded |
| Memory impairment | Not recorded |
| Mental deterioration | Not recorded |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Gaze-evoked nystagmus | Sometimes (5–29%) |
| Saccadic smooth pursuit interruptions | Sometimes (5–29%) |
| Involuntary, rapid, rhythmic eye movements | Not recorded |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Abnormality of the Achilles tendon | Often (30–79%) |
| Hyporeflexia of lower limbs | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Generalized decreased muscle tone | Often (30–79%) |
| Rigidity | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Involuntary facial quivering | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Poor swallowing | Not recorded |
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 PRKCG and how often each is seen. Find out more at hpo.jax.org.
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