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Cerebellar cystHP:0002350
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Read the genes linked to Cerebellar cyst, and the rest of your genome, with one test.
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Get my Genome Test27 genes linked to Cerebellar cyst
Changes in these genes cause rare conditions in which Cerebellar cyst 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 |
|---|---|---|
| FKRPfukutin related protein | Always | In 4 conditions |
| LAMA1laminin subunit alpha 1 | Very often (80–99%) | In 2 conditions |
| DAG1dystroglycan 1 | Often (30–79%) | In 2 conditions |
| AGTPBP1ATP/GTP binding carboxypeptidase 1 | Sometimes (5–29%) | In 1 condition |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| CRPPACDP-L-ribitol pyrophosphorylase A | Sometimes (5–29%) | In 1 condition |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Sometimes (5–29%) | In 1 condition |
| EXOSC3exosome component 3 | Sometimes (5–29%) | In 2 conditions |
| EXOSC8exosome component 8 | Sometimes (5–29%) | In 1 condition |
| EXOSC9exosome component 9 | Sometimes (5–29%) | In 1 condition |
| FKTNfukutin | Sometimes (5–29%) | In 2 conditions |
| GMPPBGDP-mannose pyrophosphorylase B | Sometimes (5–29%) | In 1 condition |
| LONP1lon peptidase 1, mitochondrial | Sometimes (5–29%) | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Sometimes (5–29%) | In 1 condition |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Sometimes (5–29%) | In 1 condition |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Sometimes (5–29%) | In 3 conditions |
| POMKprotein O-mannose kinase | Sometimes (5–29%) | In 1 condition |
| POMT1protein O-mannosyltransferase 1 | Sometimes (5–29%) | In 2 conditions |
| POMT2protein O-mannosyltransferase 2 | Sometimes (5–29%) | In 2 conditions |
| SLC25A46solute carrier family 25 member 46 | Sometimes (5–29%) | In 1 condition |
| VRK1VRK serine/threonine kinase 1 | Sometimes (5–29%) | In 1 condition |
| SEPSECSSep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase | Rarely (1–4%) | In 1 condition |
| TSEN15tRNA splicing endonuclease subunit 15 | Rarely (1–4%) | In 1 condition |
| TSEN2tRNA splicing endonuclease subunit 2 | Rarely (1–4%) | In 1 condition |
| TSEN34tRNA splicing endonuclease subunit 34 | Rarely (1–4%) | In 1 condition |
| TSEN54tRNA splicing endonuclease subunit 54 | Rarely (1–4%) | In 1 condition |
| COL3A1collagen type III alpha 1 chain | 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.
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