How genetic differences change tissue factor, a key blood clotting protein

Genetic architecture of tissue factor expression

NIH-funded research Beth Israel Deaconess Medical Center · NIH-11145263

This project looks at whether rare genetic changes in the gene for tissue factor affect blood clotting and bleeding risk in people.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBeth Israel Deaconess Medical Center NIH-funded
Lab location1 site (Boston, United States)
Project IDNIH-11145263 on NIH RePORTER

What this research studies

Researchers will search for rare DNA changes in the F3 gene that controls tissue factor and study how those changes alter tissue factor levels or function. They will examine the gene's promoter, coding sequence, and 3' untranslated region, including how microRNAs can turn the gene down, using lab biochemical tests and molecular assays. The team will combine those lab results with human genetic data and samples to link specific variants to histories of clotting (like heart attack, stroke, or VTE) or unexplained bleeding. The work aims to find people whose clotting risk is driven by previously undetected genetic changes in tissue factor.

Who could benefit from this research

Good fit: Ideal candidates would include people with unexplained blood clots (heart attack, stroke, venous thromboembolism), unexplained bleeding, or a family history of clotting or bleeding disorders who can provide genetic samples and medical history.

Not a fit: People whose bleeding or clotting problems are already explained by other diagnosed conditions or who are currently on anticoagulant therapy for clearly identified causes may not gain direct benefit from this project.

Why it matters

Potential benefit: If successful, this work could reveal genetic causes of abnormal clotting or bleeding and help identify people at higher or lower risk so care can be personalized.

How similar studies have performed: Prior research has connected tissue factor levels to clotting risk and has begun to map regulatory microRNAs, but applying rare human variant discovery across promoter, coding, and 3'UTR regions in this integrated way is relatively new.

Where this research is happening

Boston, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.