Trait
Gastrointestinal inflammation
Inflammation of the alimentary part of the gastrointestinal system.
Summary
- Also called
- GI inflammation
Reference genomeGRCh38hg38
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Get my Genome Test14 genes linked to Gastrointestinal inflammation
Changes in these genes cause rare conditions in which Gastrointestinal inflammation 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 |
|---|---|---|
| COL7A1collagen type VII alpha 1 chain | Very often (80–99%) | In 4 conditions |
| MMP1matrix metallopeptidase 1 | Very often (80–99%) | In 1 condition |
| LAMA3laminin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| IL12Ainterleukin 12A | Rarely (1–4%) | In 1 condition |
| IL12RB1interleukin 12 receptor subunit beta 1 | Rarely (1–4%) | In 1 condition |
| IRF5interferon regulatory factor 5 | Rarely (1–4%) | In 1 condition |
| MMEL1membrane metalloendopeptidase like 1 | Rarely (1–4%) | In 1 condition |
| POU2AF1POU class 2 homeobox associating factor 1 | Rarely (1–4%) | In 1 condition |
| SPIBSpi-B transcription factor | Rarely (1–4%) | In 1 condition |
| TNFSF15TNF superfamily member 15 | Rarely (1–4%) | In 1 condition |
| TNPO3transportin 3 | Rarely (1–4%) | In 1 condition |
| COL17A1collagen type XVII alpha 1 chain | Not recorded | 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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