Trait
Food allergy
Primary food allergies primarily occur as a result (most likely) of gastrointestinal sensitization to predominantly stable food allergens (glycoproteins). A secondary food allergy develops after primary sensitization to airborne allergens (e. g., pollen allergens) with subsequent reactions (due to cross-reactivity) to structurally related often labile allergens in (plant) foods.
Summary
- Also called
- Allergic reaction to foods, IgE-mediated food allergy, Immunoglobulin E-mediated food allergy, Reaction to food allergens
- Body system
- Abnormality of the immune system
Read the genes linked to Food allergy, and the rest of your genome, with one test.
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Get my Genome Test21 genes linked to Food allergy
Changes in these genes cause rare conditions in which Food allergy is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| DSG1desmoglein 1 | Always | In 1 condition |
| IL6STinterleukin 6 cytokine family signal transducer | Always | In 2 conditions |
| JAK1Janus kinase 1 | Always | In 1 condition |
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| POLD3DNA polymerase delta 3, accessory subunit | Always | In 1 condition |
| DOCK8dedicator of cytokinesis 8 | Very often (80–99%) | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Very often (80–99%) | In 2 conditions |
| STAT6signal transducer and activator of transcription 6 | Very often (80–99%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Often (30–79%) | In 1 condition |
| CARD11caspase recruitment domain family member 11 | Often (30–79%) | In 1 condition |
| FOXP3forkhead box P3 | Often (30–79%) | In 1 condition |
| ITGAVintegrin subunit alpha V | Often (30–79%) | In 1 condition |
| PGM3phosphoglucomutase 3 | Often (30–79%) | In 1 condition |
| SLC19A1solute carrier family 19 member 1 | Often (30–79%) | In 1 condition |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Sometimes (5–29%) | In 1 condition |
| PORCNporcupine O-acyltransferase | Sometimes (5–29%) | In 1 condition |
| SLC27A4solute carrier family 27 member 4 | Sometimes (5–29%) | In 1 condition |
| SOX6SRY-box transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | Rarely (1–4%) | In 1 condition |
| IGKCimmunoglobulin kappa constant | Rarely (1–4%) | In 1 condition |
| SPTBN1spectrin beta, non-erythrocytic 1 | Rarely (1–4%) | In 1 condition |
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.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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