| ID | Sequence | Length | GC content |
|---|---|---|---|
| GAGGCCCUGACGUGGACACACUUCGGGUUUCACGACUCCGGGUUUCUCC… | 8558 nt | 0.3892 | |
| CUUACUGCCCCCAUCCGGUUCGGGGAGGUGGCGGGACCUUGGCGGCGCC… | 8409 nt | 0.3846 | |
| GCUUGCCCGGGUUCCUCGGACUGCCGACGGCAGGCGUGGGUGGGUGGGU… | 8413 nt | 0.3835 | |
| CUUACUGCCCCCAUCCGGUUCGGGGAGGUGGCGGGACCUUGGCGGCGCC… | 8536 nt | 0.3899 | |
| GAGGUGCUCACUGCGCAUGUGCGCGCGCUAGAAAAGGUGGACAAGUCCU… | 8348 nt | 0.3816 |
This gene encodes a protein that belongs to a family of apoptotic suppressor proteins. Members of this family share a conserved motif termed, baculovirus IAP repeat, which is necessary for their anti-apoptotic function. This protein functions through binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2 and inhibits apoptosis induced by menadione, a potent inducer of free radicals, and interleukin 1-beta converting enzyme. This protein also inhibits at least two members of the caspase family of cell-death proteases, caspase-3 and caspase-7. Mutations in this gene are the cause of X-linked lymphoproliferative syndrome. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 2 and 11.[provided by RefSeq, Feb 2011]
A study in human cadaver liver tissues demonstrated that the XIAP was up-regulated greater than 28-fold in decaying tissues compared to a control, as part of the apoptotic thanatotranscriptome where pro-apoptotic genes were generally up-regulated over a 48-hour postmortem interval [Javan et al. DOI:10.1007/S12024-015-9704-6]. Research in human postmortem prostate tissues further showed that the XIAP was significantly up-regulated in a time-dependent manner, with its expression significantly elevated at longer postmortem intervals alongside other anti-apoptotic genes [Tolbert et al. DOI:10.1016/j.gene.2018.06.090].