| ID | Sequence | Length | GC content |
|---|---|---|---|
| GCCGCGUUGCGCUCCCGCCACUCCGCGCCCGCUAUCCUGGCUCCGUGCU… | 2536 nt | 0.5931 | |
| GCCGCGUUGCGCUCCCGCCACUCCGCGCCCGCUAUCCUGGCUCCGUGCU… | 2371 nt | 0.5972 | |
| GCCGCGUUGCGCUCCCGCCACUCCGCGCCCGCUAUCCUGGCUCCGUGCU… | 2255 nt | 0.5956 | |
| CUCACACUUAGAAACUCCCGGUGUGGCAGCUGAGAUGGCCCAGGAAAGA… | 2600 nt | 0.5804 | |
| AGACACAGAGACAGACGCCAGAGAGGAAGGCAGACAAAGAGACGGGUGG… | 2534 nt | 0.5864 | |
| AGACACAGAGACAGACGCCAGAGAGGAAGGCAGACAAAGAGACGGGUGG… | 2569 nt | 0.5858 |
This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatase s: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015]
A study in humans demonstrated that plasma exosomal mRNA profiles, assessed via RNA sequencing, can distinguish acute myocardial infarction (AMI) patients from stable coronary artery disease patients and healthy controls [He et al. DOI:10.3389/fcvm.2021.712061].