| ID | Sequence | Length | GC content |
|---|---|---|---|
| GGAACAGCGGCCUCUGACACCAGCACAGCAAACCCGCCGGGAUCAAAGU… | 1536 nt | 0.5658 | |
| GGAACAGCGGCCUCUGACACCAGCACAGCAAACCCGCCGGGAUCAAAGU… | 1931 nt | 0.5805 | |
| GGAACAGCGGCCUCUGACACCAGCACAGCAAACCCGCCGGGAUCAAAGU… | 1722 nt | 0.5708 |
This gene encodes a member of the selenium-binding protein family. Selenium is an essential nutrient that exhibits potent anticarcinogenic properties, and deficiency of selenium may cause certain neurologic diseases. The effects of selenium in preventing cancer and neurologic diseases may be mediated by selenium-binding proteins, and decreased expression of this gene may be associated with several types of cancer. The encoded protein may play a selenium-dependent role in ubiquitination/deubiquitination-mediated protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]
A study in humans demonstrated that the SELENBP1 shows high sensitivity and specificity rates in cases of death caused by coronary artery spasm [Cătinas et al. DOI:10.3390/ijms26146818]. A study in humans demonstrated that the SELENBP1 shows high sensitivity and specificity rates in cases of death caused by coronary artery spasm [Cătinas and Hostiuc DOI:10.3390/ijms26146818].