RPS26P11 gene homepage

General information
Gene symbol RPS26P11
Gene name ribosomal protein S26 pseudogene 11
Chromosome X
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NG_021430.1
Transcript reference NR_002309.1
Associated with diseases -
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 2
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 17, 2010
Date last updated July 30, 2018
Version RPS26P11:180730

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 31817
Entrez Gene 441502
PubMed articles RPS26P11


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00018209 X ribosomal protein S26 pseudogene 11 NR_002309.1 - 2


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