The RPS4X gene homepage

General information
Gene symbol RPS4X
Gene name ribosomal protein S4, X-linked
Chromosome X
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NG_012524.1
Transcript reference NM_001007.4
Exon/intron information NM_001007.4 exon/intron table
Associated with diseases -
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 16
Unique public DNA variants reported 8
Individuals with public variants 120
Hidden variants 5
Download all this gene's data Download all data
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 July 21, 2020
Version RPS4X:200721

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_001007.4.
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
Homepage URL https://www.LOVD.nl/RPS4X
HGNC 10424
Entrez Gene 6191
PubMed articles RPS4X
OMIM - Gene 312760
HGMD RPS4X
GeneCards RPS4X
GeneTests RPS4X
Orphanet RPS4X


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000626 X ribosomal protein S4, X-linked NM_001007.4 NP_000998.1 16


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