| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGAGACUGCGAGAAGGAGGUCCCCCACGGCCCUUCAGGAUGAAAGCUGC… | 899 nt | 0.6296 | |
| AGAGACUGCGAGAAGGAGGUGCGUCCUGCUGCCUGCCCCGGUCACUCUG… | 976 nt | 0.6363 | |
| AGAGACUGCGAGAAGGAGGUGCGUCCUGCUGCCUGCCCCGGUCACUCUG… | 945 nt | 0.6328 | |
| CACAAUGGACAAUGGCAACUGCCCACACACUCCCAUGGAGGGGAAGGGG… | 1195 nt | 0.6201 | |
| AGAGACUGCGAGAAGGAGGUGCGUCCUGCUGCCUGCCCCGGUCACUCUG… | 985 nt | 0.6355 | |
| AGAGACUGCGAGAAGGAGGUCCCCCACGGCCCUUCAGGAUGAAAGCUGC… | 891 nt | 0.6285 |
This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein. [provided by RefSeq, Dec 2015]
A study in pigs demonstrated that the APOA1 gene expression in subcutaneous fat tissue from bruises was down-regulated over time following a high-force impact [Barington et al. DOI:10.007/s12024-017-9869-2]. Another study in porcine bruises confirmed the APOA1 was downregulated over time relative to control tissue [Barington et al. DOI:10.1016/J.Jflm.2018.06.005]. A study in humans demonstrated that changes in the isoform distribution of the APOA1 were observed in serum following treatment with human growth hormone and administration of the GHRH analog CJC-1295 [Reichel DOI:10.1016/J.Forsciint.2011.07.031].