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Traits
Traits linked to STAT6
signal transducer and activator of transcription 6
The Human Phenotype Ontology links 44 traits to STAT6, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Gastrointestinal eosinophilia | Often (30–79%) |
| Acid reflux | Sometimes (5–29%) |
| Abnormal peritoneum morphology | Rarely (1–4%) |
| Constipation | Rarely (1–4%) |
| Liver cancer | Rarely (1–4%) |
| Pelvic mass | Rarely (1–4%) |
| Eosinophilic infiltration of the esophagus | Not recorded |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Baby eczema | Very often (80–99%) |
| Food allergy | Very often (80–99%) |
| Anaphylaxis | Often (30–79%) |
| Asthma | Often (30–79%) |
| Recurrent respiratory infections | Often (30–79%) |
| Recurrent skin infections | Often (30–79%) |
| Recurrent viral infections | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Genital tumor | Sometimes (5–29%) |
| Abnormality of the prostate | Rarely (1–4%) |
| Prostate cancer | Rarely (1–4%) |
| Urinary retention | Rarely (1–4%) |
| Uterine cancer | Rarely (1–4%) |
| Vaginal tumor | Rarely (1–4%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Decreased circulating C-peptide concentration | Rarely (1–4%) |
| Fever | Rarely (1–4%) |
| Low blood sugar | Rarely (1–4%) |
| Recurrent low blood sugar levels | Rarely (1–4%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Osteoporosis | Sometimes (5–29%) |
| Hypophosphatemic rickets | Rarely (1–4%) |
| Lumbago | Rarely (1–4%) |
Abnormal tissue mass
| Trait | How often it is seen |
|---|---|
| Abnormal tissue mass | Sometimes (5–29%) |
| Soft tissue neoplasm | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| High blood eosinophil count | Very often (80–99%) |
| B-cell lymphoma | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Loss of consciousness | Rarely (1–4%) |
| Nervous system cancer | Rarely (1–4%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Neoplasia of the pleura | Sometimes (5–29%) |
| Lung cancer | Rarely (1–4%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Sometimes (5–29%) |
| Night sweats | Rarely (1–4%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Short stature | Often (30–79%) |
| Weight loss | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Increased circulating IgE concentration | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormality of the forehead | Rarely (1–4%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Hypoinsulinemia | Rarely (1–4%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Double vision | Rarely (1–4%) |
Abnormality of the thoracic cavity
| Trait | How often it is seen |
|---|---|
| Abnormal mediastinum morphology | Rarely (1–4%) |
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 STAT6 and how often each is seen. Find out more at hpo.jax.org.
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