Trait
Broad ribs
Increased width of ribs
Summary
- Also called
- Wide ribs
- 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.
library(jsonlite)
url <- "https://dantelabs.com/traits/broad-ribs.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Broad ribs, and the rest of your genome, with one test.
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Get my Genome Test25 genes linked to Broad ribs
Changes in these genes cause rare conditions in which Broad ribs 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 |
|---|---|---|
| ARSKarylsulfatase family member K | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| IL1RNinterleukin 1 receptor antagonist | Always | In 1 condition |
| PTDSS1phosphatidylserine synthase 1 | Always | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Always | In 1 condition |
| SERPINH1serpin family H member 1 | Always | In 1 condition |
| TMEM53transmembrane protein 53 | Always | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Very often (80–99%) | In 1 condition |
| COL11A2collagen type XI alpha 2 chain | Very often (80–99%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Often (30–79%) | In 1 condition |
| DYMdymeclin | Often (30–79%) | In 1 condition |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Often (30–79%) | In 1 condition |
| NEK9NIMA related kinase 9 | Often (30–79%) | In 1 condition |
| SETBP1SET binding protein 1 | Often (30–79%) | In 2 conditions |
| SMAD4SMAD family member 4 | Often (30–79%) | In 1 condition |
| TFE3transcription factor binding to IGHM enhancer 3 | Often (30–79%) | In 1 condition |
| WNT7AWnt family member 7A | Often (30–79%) | In 1 condition |
| XYLT1xylosyltransferase 1 | Often (30–79%) | In 1 condition |
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Not recorded | In 1 condition |
| AMER1APC membrane recruitment protein 1 | Not recorded | In 1 condition |
| ARSBarylsulfatase B | Not recorded | In 1 condition |
| ATP7AATPase copper transporting alpha | Not recorded | In 1 condition |
| FBN1fibrillin 1 | Not recorded | In 1 condition |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Not recorded | In 1 condition |
| SOSTsclerostin | 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 2026.10.17-8666dff2.
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