Trait
Biliary tract abnormality
An abnormality of the biliary tree.
Summary
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
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Get my Genome Test16 genes linked to Biliary tract abnormality
Changes in these genes cause rare conditions in which Biliary tract abnormality 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 |
|---|---|---|
| ABCC2ATP binding cassette subfamily C member 2 | Very often (80–99%) | In 2 conditions |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Very often (80–99%) | In 1 condition |
| UGT1A1UDP glucuronosyltransferase family 1 member A1 | Very often (80–99%) | In 1 condition |
| CPLX1complexin 1 | Sometimes (5–29%) | In 1 condition |
| CTBP1C-terminal binding protein 1 | Sometimes (5–29%) | In 1 condition |
| FGFRL1fibroblast growth factor receptor like 1 | Sometimes (5–29%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Sometimes (5–29%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Sometimes (5–29%) | In 1 condition |
| ARL6ARF like GTPase 6 | Not recorded | In 1 condition |
| B3GLCTbeta 3-glucosyltransferase | Not recorded | In 1 condition |
| BBS1Bardet-Biedl syndrome 1 | Not recorded | In 1 condition |
| CCDC28Bcoiled-coil domain containing 28B | Not recorded | In 1 condition |
| CIITAclass II major histocompatibility complex transactivator | Not recorded | In 1 condition |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Not recorded | In 1 condition |
| HNF1BHNF1 homeobox B | Not recorded | In 1 condition |
| STK11serine/threonine kinase 11 | 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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