Trait
Coronal cleft vertebrae
Frontal schisis (cleft or cleavage) of vertebral bodies.
Summary
- Also called
- coronal cleft of vertebrae, Coronal clefts, Coronal vertebral clefts, Vertebral coronal clefts
- Body system
- Abnormality of the musculoskeletal system
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
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page$trait$nameRead the genes linked to Coronal cleft vertebrae, and the rest of your genome, with one test.
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Get my Genome Test18 genes linked to Coronal cleft vertebrae
Changes in these genes cause rare conditions in which Coronal cleft vertebrae 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 |
|---|---|---|
| COL2A1collagen type II alpha 1 chain | Always | In 2 conditions |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Always | In 1 condition |
| FLNBfilamin B | Always | In 3 conditions |
| GNPATglyceronephosphate O-acyltransferase | Always | In 1 condition |
| HSPA9heat shock protein family A (Hsp70) member 9 | Always | In 1 condition |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Always | In 1 condition |
| LONP1lon peptidase 1, mitochondrial | Very often (80–99%) | In 2 conditions |
| ALDH1A2aldehyde dehydrogenase 1 family member A2 | Often (30–79%) | In 1 condition |
| HSPG2heparan sulfate proteoglycan 2 | Often (30–79%) | In 1 condition |
| LAMA5laminin subunit alpha 5 | Often (30–79%) | In 1 condition |
| ARSLarylsulfatase L | Sometimes (5–29%) | In 1 condition |
| COL11A2collagen type XI alpha 2 chain | Sometimes (5–29%) | In 2 conditions |
| SLC10A7solute carrier family 10 member 7 | Sometimes (5–29%) | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Sometimes (5–29%) | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Not recorded | In 1 condition |
| PEX7peroxisomal biogenesis factor 7 | Not recorded | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Not recorded | In 1 condition |
| TRIP11thyroid hormone receptor interactor 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.
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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