| ID | Sequence | Length | GC content |
|---|---|---|---|
| AACCGUAACAGCCACCAGACAAGCUUCAGUGGCCGGCCCUUCACAUCCA… | 2127 nt | 0.5806 | |
| AACCGUAACAGCCACCAGACAAGCUUCAGUGGCCGGCCCUUCACAUCCA… | 2046 nt | 0.5787 | |
| AACCGUAACAGCCACCAGACAAGCUUCAGUGGCCGGCCCUUCACAUCCA… | 1671 nt | 0.5703 |
This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Feb 2011]
The protein marker ECM1 (Extracellular matrix protein 1) serves as an indicator of cardiorespiratory fitness (CRF) in human plasma, as identified in donor profiling studies [Alex et al. DOI:10.1016/j.scijus.2025.101320]. A review of wound age estimation studies in human, mouse, and rat skin wounds indicates that the ECM1 is an extracellular matrix protein whose presence or absence provides temporal information for forensic wound dating [Cecchi DOI:10.1007/S00414-010-0505-X].