Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test26 genes linked to Liver cysts
Changes in these genes cause rare conditions in which Liver cysts 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 |
|---|---|---|
| ALG8ALG8 alpha-1,3-glucosyltransferase | Always | In 1 condition |
| ALPK3alpha kinase 3 | Always | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Always | In 1 condition |
| CILK1ciliogenesis associated kinase 1 | Always | In 1 condition |
| JAK1Janus kinase 1 | Always | In 1 condition |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Very often (80–99%) | In 1 condition |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Very often (80–99%) | In 2 conditions |
| BICC1BicC family RNA binding protein 1 | Very often (80–99%) | In 1 condition |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Very often (80–99%) | In 2 conditions |
| GANABglucosidase II alpha subunit | Very often (80–99%) | In 2 conditions |
| IFT140intraflagellar transport 140 | Very often (80–99%) | In 2 conditions |
| NEK8NIMA related kinase 8 | Very often (80–99%) | In 4 conditions |
| PKD1polycystin 1, transient receptor potential channel interacting | Very often (80–99%) | In 2 conditions |
| PKD2polycystin 2, transient receptor potential cation channel | Very often (80–99%) | In 2 conditions |
| EXTL3exostosin like glycosyltransferase 3 | Often (30–79%) | In 1 condition |
| LRP5LDL receptor related protein 5 | Often (30–79%) | In 1 condition |
| TTC21Btetratricopeptide repeat domain 21B | Often (30–79%) | In 1 condition |
| WDR19WD repeat domain 19 | Often (30–79%) | In 2 conditions |
| IFNGinterferon gamma | Sometimes (5–29%) | In 1 condition |
| NPHP3nephrocystin 3 | Sometimes (5–29%) | In 2 conditions |
| OFD1OFD1 centriole and centriolar satellite protein | Sometimes (5–29%) | In 1 condition |
| TSC1TSC complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| TSC2TSC complex subunit 2 | Sometimes (5–29%) | In 1 condition |
| IFT122intraflagellar transport 122 | Not recorded | In 1 condition |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Not recorded | In 1 condition |
| SEC63SEC63 protein translocation regulator | 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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