Trait
Bile duct inflammation
Clinical name: Cholangitis
Inflammation of the biliary ductal system, affecting the intrahepatic or extrahepatic portions, or both.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Bile duct inflammation, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test20 genes linked to Bile duct inflammation
Changes in these genes cause rare conditions in which Bile duct 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 |
|---|---|---|
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| IL21Rinterleukin 21 receptor | Always | In 1 condition |
| OAS22'-5'-oligoadenylate synthetase 2 | Always | In 1 condition |
| PSKH1protein serine kinase H1 | Always | In 1 condition |
| RELREL proto-oncogene, NF-kB subunit | Always | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Often (30–79%) | In 1 condition |
| BCAP31B cell receptor associated protein 31 | Often (30–79%) | In 1 condition |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Often (30–79%) | In 2 conditions |
| ABCB4ATP binding cassette subfamily B member 4 | Sometimes (5–29%) | In 2 conditions |
| DZIP1LDAZ interacting zinc finger protein 1 like | Sometimes (5–29%) | In 1 condition |
| IL36RNinterleukin 36 receptor antagonist | Sometimes (5–29%) | In 1 condition |
| ITCHitchy E3 ubiquitin protein ligase | Sometimes (5–29%) | In 1 condition |
| MED12mediator complex subunit 12 | Sometimes (5–29%) | In 1 condition |
| XIAPX-linked inhibitor of apoptosis | 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 |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Not recorded | In 1 condition |
| CIITAclass II major histocompatibility complex transactivator | Not recorded | In 1 condition |
| WDR35WD repeat domain 35 | 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