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Trait
Thin ribs
Ribs with a reduced diameter.
Summary
- Also called
- Slender ribs
- Body system
- Abnormality of the musculoskeletal system
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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/thin-ribs.json"
page <- fromJSON(url)
page$trait$nameThin ribsHP:0000883
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Get my Genome Test54 genes linked to Thin ribs
Changes in these genes cause rare conditions in which Thin 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 |
|---|---|---|
| COL1A1collagen type I alpha 1 chain | Always | In 2 conditions |
| COL1A2collagen type I alpha 2 chain | Always | In 2 conditions |
| DNM2dynamin 2 | Always | In 2 conditions |
| DONSONDNA replication fork stabilization factor DONSON | Always | In 1 condition |
| P3H1prolyl 3-hydroxylase 1 | Always | In 1 condition |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Always | In 1 condition |
| SERPINH1serpin family H member 1 | Always | In 1 condition |
| TOMM7translocase of outer mitochondrial membrane 7 | Always | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | Very often (80–99%) | In 1 condition |
| BANF1barrier to autointegration nuclear assembly factor 1 | Often (30–79%) | In 1 condition |
| BIN1bridging integrator 1 | Often (30–79%) | In 1 condition |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Often (30–79%) | In 1 condition |
| CUL7cullin 7 | Often (30–79%) | In 1 condition |
| HDAC6histone deacetylase 6 | Often (30–79%) | In 2 conditions |
| LAMA5laminin subunit alpha 5 | Often (30–79%) | In 1 condition |
| MTMR14myotubularin related protein 14 | Often (30–79%) | In 1 condition |
| MYF6myogenic factor 6 | Often (30–79%) | In 1 condition |
| OBSL1obscurin like cytoskeletal adaptor 1 | Often (30–79%) | In 2 conditions |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 1 condition |
| SCARF2scavenger receptor class F member 2 | Often (30–79%) | In 2 conditions |
| TBCEtubulin folding cofactor E | Often (30–79%) | In 2 conditions |
| ACTA1actin alpha 1, skeletal muscle | Sometimes (5–29%) | In 1 condition |
| KLHL40kelch like family member 40 | Sometimes (5–29%) | In 1 condition |
| KLHL41kelch like family member 41 | Sometimes (5–29%) | In 1 condition |
| LMOD3leiomodin 3 | Sometimes (5–29%) | In 1 condition |
| MAMLD1mastermind like domain containing 1 | Sometimes (5–29%) | In 1 condition |
| MTM1myotubularin 1 | Sometimes (5–29%) | In 1 condition |
| MTX2metaxin 2 | Sometimes (5–29%) | In 1 condition |
| NEBnebulin | Sometimes (5–29%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Sometimes (5–29%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sometimes (5–29%) | In 1 condition |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Sometimes (5–29%) | In 1 condition |
| USP18ubiquitin specific peptidase 18 | Sometimes (5–29%) | In 1 condition |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Not recorded | In 1 condition |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Not recorded | In 1 condition |
| CHRNDcholinergic receptor nicotinic delta subunit | Not recorded | In 1 condition |
| CHRNGcholinergic receptor nicotinic gamma subunit | Not recorded | In 1 condition |
Show 14 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| COL11A1collagen type XI alpha 1 chain | Not recorded | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Not recorded | In 1 condition |
| EXOC6Bexocyst complex component 6B | Not recorded | In 1 condition |
| FAM111AFAM111 trypsin like peptidase A | Not recorded | In 1 condition |
| LIFRLIF receptor subunit alpha | Not recorded | In 1 condition |
| MUSKmuscle associated receptor tyrosine kinase | Not recorded | In 1 condition |
| ORC1origin recognition complex subunit 1 | Not recorded | In 1 condition |
| POLR3ARNA polymerase III subunit A | Not recorded | In 1 condition |
| RTTNrotatin | Not recorded | In 1 condition |
| SEC24DSEC24 homolog D, COPII component | Not recorded | In 1 condition |
| SKISKI proto-oncogene | Not recorded | In 1 condition |
| SOX9SRY-box transcription factor 9 | Not recorded | In 1 condition |
| TENT5Aterminal nucleotidyltransferase 5A | Not recorded | In 1 condition |
| WNT1Wnt family member 1 | 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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