Trait
Gallbladder inflammation
Clinical name: Cholecystitis
The presence of inflammatory changes in the gallbladder.
Summary
- Also called
- Recurrent cholecystitis, Unusual cholecystitis
Reference genomeGRCh38hg38
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Get my Genome Test22 genes linked to Gallbladder inflammation
Changes in these genes cause rare conditions in which Gallbladder 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 |
|---|---|---|
| PAN2poly(A) specific ribonuclease subunit PAN2 | Always | In 1 condition |
| POT1protection of telomeres 1 | Always | In 1 condition |
| TMEM63Btransmembrane protein 63B | Always | In 1 condition |
| TFE3transcription factor binding to IGHM enhancer 3 | Often (30–79%) | In 1 condition |
| ABCB4ATP binding cassette subfamily B member 4 | Sometimes (5–29%) | In 3 conditions |
| ARSAarylsulfatase A | Sometimes (5–29%) | In 4 conditions |
| CALRcalreticulin | Sometimes (5–29%) | In 1 condition |
| F5coagulation factor V | Sometimes (5–29%) | In 1 condition |
| GPIglucose-6-phosphate isomerase | Sometimes (5–29%) | In 2 conditions |
| JAK2Janus kinase 2 | Sometimes (5–29%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Sometimes (5–29%) | In 1 condition |
| PSAPprosaposin | Sometimes (5–29%) | In 3 conditions |
| ABCB11ATP binding cassette subfamily B member 11 | Rarely (1–4%) | In 1 condition |
| ATP8B1ATPase phospholipid transporting 8B1 | Rarely (1–4%) | 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 |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Rarely (1–4%) | In 1 condition |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Rarely (1–4%) | In 1 condition |
| ALDOAaldolase, fructose-bisphosphate A | Not recorded | In 1 condition |
| HK1hexokinase 1 | Not recorded | In 1 condition |
| PKLRpyruvate kinase L/R | Not recorded | In 1 condition |
| TPI1triosephosphate isomerase 1 | 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.
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.
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