Trait
Parietal bossing
Parietal bossing is a marked prominence in the parietal region.
Summary
- Also called
- Biparietal bossing, Bossing of parietal bone
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test9 genes linked to Parietal bossing
Changes in these genes cause rare conditions in which Parietal bossing 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 |
|---|---|---|
| FIG4FIG4 phosphoinositide 5-phosphatase | Always | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Always | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Often (30–79%) | In 1 condition |
| MPDU1mannose-P-dolichol utilization defect 1 | Often (30–79%) | In 2 conditions |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Sometimes (5–29%) | In 1 condition |
| POLR3ARNA polymerase III subunit A | Not recorded | In 1 condition |
| PTCH1patched 1 | Not recorded | In 2 conditions |
| PTPN11protein tyrosine phosphatase non-receptor type 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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