Basic Information

Symbol
XIAP
RNA class
mRNA
Alias
X-Linked Inhibitor Of Apoptosis BIRC4 HILP API3 X-Linked Inhibitor Of Apoptosis, E3 Ubiquitin Protein Ligase Baculoviral IAP Repeat-Containing Protein 4 RING-Type E3 Ubiquitin Transferase XIAP E3 Ubiquitin-Protein Ligase XIAP Inhibitor Of Apoptosis Protein 3 IAP-Like Protein 1 X-Linked IAP HIAP-3 ILP-1 IAP-3 HIAP3 X-Linked Inhibitor Of Apoptosis Protein Baculoviral IAP Repeat-Containing 4 IAP-Like Protein EC 2.3.2.27 ILP1 MIHA XLP2 IAP3 ILP
Location (GRCh38)
Forensic tag(s)
Postmortem interval inference

MANE select

Transcript ID
NM_001167.4
Sequence length
8558.0 nt
GC content
0.3892

Transcripts

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
Summary

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]

Forensic Context

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].