Trait
Increased mobility in finger joint
Clinical name: Finger joint hypermobility
Summary
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/finger-joint-hypermobility.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Increased mobility in finger joint, and the rest of your genome, with one test.
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Get my Genome Test19 genes linked to Increased mobility in finger joint
Changes in these genes cause rare conditions in which Increased mobility in finger joint 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 |
|---|---|---|
| B3GALT6beta-1,3-galactosyltransferase 6 | Always | In 2 conditions |
| COL1A1collagen type I alpha 1 chain | Always | In 1 condition |
| COL3A1collagen type III alpha 1 chain | Always | In 1 condition |
| COL6A2collagen type VI alpha 2 chain | Always | In 1 condition |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Always | In 1 condition |
| ERI1exoribonuclease 1 | Always | In 1 condition |
| ESAMendothelial cell adhesion molecule | Always | In 1 condition |
| HIVEP2HIVEP zinc finger 2 | Always | In 1 condition |
| NLRP1NLR family pyrin domain containing 1 | Always | In 1 condition |
| P4HTMprolyl 4-hydroxylase, transmembrane | Always | In 1 condition |
| PPIBpeptidylprolyl isomerase B | Always | In 1 condition |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Always | In 1 condition |
| SLC13A1solute carrier family 13 member 1 | Always | In 1 condition |
| CBLCbl proto-oncogene | Often (30–79%) | In 1 condition |
| HYAL1hyaluronidase 1 | Often (30–79%) | In 1 condition |
| COMPcartilage oligomeric matrix protein | Sometimes (5–29%) | In 1 condition |
| PROKR2prokineticin receptor 2 | Sometimes (5–29%) | In 1 condition |
| RNF13ring finger protein 13 | Sometimes (5–29%) | In 1 condition |
| YY1YY1 transcription factor | Sometimes (5–29%) | In 2 conditions |
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.
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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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