CXorf22 gene homepage

General information
Gene symbol CXorf22
Gene name chromosome X open reading frame 22
Chromosome X
Chromosomal band p21.1
Imprinted Unknown
Genomic reference NG_021289.1
Transcript reference NM_152632.3
Associated with diseases -
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 14
Unique public DNA variants reported 13
Individuals with public variants 62
Hidden variants 0
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 March 06, 2009
Date last updated August 17, 2018
Version CXorf22:180817

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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 28546
Entrez Gene 170063
PubMed articles CXorf22


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00005939 X chromosome X open reading frame 22 NM_152632.3 NP_689845.2 14


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