Trait
Enterocolitis
An inflammation of the colon and small intestine. However, most conditions are either categorized as Enteritis (inflammation of the small intestine) or Colitis (inflammation of the large intestine).
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Enterocolitis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test28 genes linked to Enterocolitis
Changes in these genes cause rare conditions in which Enterocolitis 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 |
|---|---|---|
| COPZ1coat protein complex I subunit zeta 1 | Always | In 1 condition |
| IL10RAinterleukin 10 receptor subunit alpha | Always | In 1 condition |
| IL10RBinterleukin 10 receptor subunit beta | Always | In 1 condition |
| NOP10NOP10 ribonucleoprotein | Always | In 1 condition |
| PIK3CGphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | Always | In 1 condition |
| PLCG2phospholipase C gamma 2 | Always | In 1 condition |
| SPOUT1SPOUT domain containing methyltransferase 1 | Always | In 1 condition |
| TTC7Atetratricopeptide repeat domain 7A | Always | In 1 condition |
| DKC1dyskerin pseudouridine synthase 1 | Often (30–79%) | In 1 condition |
| STAT1signal transducer and activator of transcription 1 | Often (30–79%) | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Sometimes (5–29%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Sometimes (5–29%) | In 1 condition |
| ECE1endothelin converting enzyme 1 | Sometimes (5–29%) | In 1 condition |
| EDN3endothelin 3 | Sometimes (5–29%) | In 1 condition |
| EDNRBendothelin receptor type B | Sometimes (5–29%) | In 1 condition |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Sometimes (5–29%) | In 1 condition |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Sometimes (5–29%) | In 1 condition |
| GDNFglial cell derived neurotrophic factor | Sometimes (5–29%) | In 1 condition |
| NRTNneurturin | Sometimes (5–29%) | In 1 condition |
| OPLAH5-oxoprolinase, ATP-hydrolysing | Sometimes (5–29%) | In 2 conditions |
| RETret proto-oncogene | Sometimes (5–29%) | In 2 conditions |
| SEMA3Csemaphorin 3C | Sometimes (5–29%) | In 1 condition |
| SEMA3Dsemaphorin 3D | Sometimes (5–29%) | In 1 condition |
| SLC37A4solute carrier family 37 member 4 | Sometimes (5–29%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Sometimes (5–29%) | In 1 condition |
| SREBF1sterol regulatory element binding transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| ELANEelastase, neutrophil expressed | Rarely (1–4%) | In 1 condition |
| NLRC4NLR family CARD domain containing 4 | 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.
Narrower traits
Broader traits
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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks