Trait
Barrel-shaped chest
A rounded, bulging chest that resembles the shape of a barrel. That is, there is an increased anteroposterior diameter and usually some degree of kyphosis.
Summary
- Also called
- Barrel chest
- Body system
- Abnormality of the musculoskeletal system
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page$trait$nameRead the genes linked to Barrel-shaped chest, and the rest of your genome, with one test.
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Achondrogenesis panelReads 2 of these genesCOL2A1TRIP11About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRMRPAbout this report →
- Osteogenesis ImperfectaReads 3 of these genesKDELR2P3H1LRP5About this report →
- Familial Paget Disease of BoneReads 1 of these genesTNFRSF11BAbout this report →
Show 14 more reports
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesLRP5About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- VitreoretinopathyReads 2 of these genesCOL2A1LRP5About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesFUCA1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL2A1About this report →
- Type I InterferonopathiesReads 1 of these genesACP5About this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Noonan SyndromeReads 1 of these genesHRASAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesCOL13A1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesACP5About this report →
- Lysosomal Storage DiseaseReads 1 of these genesFUCA1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesHRASAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesTRPV4About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRMRPAbout this report →
Read the genes linked to Barrel-shaped chest, and the rest of your genome, with one test.
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Get my Genome Test23 genes linked to Barrel-shaped chest
Changes in these genes cause rare conditions in which Barrel-shaped chest 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 |
|---|---|---|
| ACANaggrecan | Always | In 2 conditions |
| DYMdymeclin | Always | In 2 conditions |
| LBRlamin B receptor | Always | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Always | In 1 condition |
| TRAPPC2trafficking protein particle complex subunit 2 | Always | In 2 conditions |
| CHST3carbohydrate sulfotransferase 3 | Very often (80–99%) | In 2 conditions |
| ACP5acid phosphatase 5, tartrate resistant | Often (30–79%) | In 1 condition |
| COL13A1collagen type XIII alpha 1 chain | Often (30–79%) | In 1 condition |
| KDELR2KDEL endoplasmic reticulum protein retention receptor 2 | Often (30–79%) | In 1 condition |
| WNT7AWnt family member 7A | Often (30–79%) | In 1 condition |
| CILK1ciliogenesis associated kinase 1 | Sometimes (5–29%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Sometimes (5–29%) | In 4 conditions |
| P3H1prolyl 3-hydroxylase 1 | Sometimes (5–29%) | In 1 condition |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Sometimes (5–29%) | In 1 condition |
| MYH3myosin heavy chain 3 | Rarely (1–4%) | In 1 condition |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Not recorded | In 1 condition |
| FUCA1alpha-L-fucosidase 1 | Not recorded | In 1 condition |
| HRASHRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| LRP5LDL receptor related protein 5 | Not recorded | In 1 condition |
| RAB33BRAB33B, member RAS oncogene family | Not recorded | In 1 condition |
| TNFRSF11BTNF receptor superfamily member 11b | Not recorded | In 1 condition |
| TRIP11thyroid hormone receptor interactor 11 | Not recorded | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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 2026.10.17-8666dff2.
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