Trait
Irregular vertebral endplates
An irregular surface of the vertebral end plates, which are normally relatively smooth.
Summary
- Also called
- end-plate irregularities, endplate irregularities, endplate irregularity, Irregular end plates, Irregular endplates, irregular vertebral plates, vertebral endplate irregularity
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Irregular vertebral endplates, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test32 genes linked to Irregular vertebral endplates
Changes in these genes cause rare conditions in which Irregular vertebral endplates 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 |
|---|---|---|
| CCN2cellular communication network factor 2 | Always | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Always | In 3 conditions |
| EXOC6Bexocyst complex component 6B | Always | In 1 condition |
| MIR140microRNA 140 | Always | In 1 condition |
| SLC13A1solute carrier family 13 member 1 | Always | In 1 condition |
| CCN6cellular communication network factor 6 | Very often (80–99%) | In 1 condition |
| COG4component of oligomeric golgi complex 4 | Very often (80–99%) | In 1 condition |
| SLC29A3solute carrier family 29 member 3 | Very often (80–99%) | In 1 condition |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Very often (80–99%) | In 1 condition |
| TNFRSF11ATNF receptor superfamily member 11a | Very often (80–99%) | In 1 condition |
| ZBTB20zinc finger and BTB domain containing 20 | Very often (80–99%) | In 2 conditions |
| COL9A1collagen type IX alpha 1 chain | Often (30–79%) | In 2 conditions |
| COL9A2collagen type IX alpha 2 chain | Often (30–79%) | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Often (30–79%) | In 1 condition |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Often (30–79%) | In 1 condition |
| LOXL3lysyl oxidase like 3 | Often (30–79%) | In 1 condition |
| COL10A1collagen type X alpha 1 chain | Sometimes (5–29%) | In 2 conditions |
| PDE4Dphosphodiesterase 4D | Sometimes (5–29%) | In 1 condition |
| SLC10A7solute carrier family 10 member 7 | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| ACP5acid phosphatase 5, tartrate resistant | Not recorded | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Not recorded | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Not recorded | In 1 condition |
| COMPcartilage oligomeric matrix protein | Not recorded | In 1 condition |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Not recorded | In 1 condition |
| GNPATglyceronephosphate O-acyltransferase | Not recorded | In 1 condition |
| GORABgolgin, RAB6 interacting | Not recorded | In 1 condition |
| KIF22kinesin family member 22 | Not recorded | In 1 condition |
| NANSN-acetylneuraminate synthase | Not recorded | In 1 condition |
| PAPSS23'-phosphoadenosine 5'-phosphosulfate synthase 2 | Not recorded | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Not recorded | In 1 condition |
| SLC39A13solute carrier family 39 member 13 | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks