The XIAP gene homepage

General information
Gene symbol XIAP
Gene name X-linked inhibitor of apoptosis
Chromosome X
Chromosomal band q25
Imprinted Unknown
Genomic reference NG_007264.1
Transcript reference NM_001167.3
Exon/intron information NM_001167.3 exon/intron table
Associated with diseases XLP1, XLP2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 61
Unique public DNA variants reported 41
Individuals with public variants 168
Hidden variants 4
Notes This gene sequence variant database has been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created May 08, 2009
Date last updated April 16, 2023
Version XIAP:230416

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001167.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 592
Entrez Gene 331
PubMed articles XIAP
OMIM - Gene 300079
OMIM - Diseases XLP1 (lymphoproliferative syndrome, X-linked, type 1 (XLP-1))
XLP2 (lymphoproliferative syndrome, X-linked, type 2 (XLP-2))
HGMD XIAP
GeneCards XIAP
GeneTests XIAP
Orphanet XIAP


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000586 X transcript variant 1 NM_001167.3 NP_001158.2 61


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