The RPL10 gene homepage

General information
Gene symbol RPL10
Gene name ribosomal protein L10
Chromosome X
Chromosomal band q28
Imprinted Unknown
Genomic reference NG_012890.2
Transcript reference NM_006013.3
Exon/intron information NM_006013.3 exon/intron table
Associated with diseases AUTSX5, MRXS35
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 78
Unique public DNA variants reported 60
Individuals with public variants 125
Hidden variants 7
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 February 26, 2024
Version RPL10:240226

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_006013.3.
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
Homepage URL https://www.LOVD.nl/RPL10
HGNC 10298
Entrez Gene 6134
PubMed articles RPL10
OMIM - Gene 312173
OMIM - Diseases AUTSX5 (autism, susceptibility to, X-linked, type 5 (AUTSX-5))
MRXS35 (mental retardation, X-linked, syndromic, type 35 (MRXS-35))
HGMD RPL10
GeneCards RPL10
GeneTests RPL10
Orphanet RPL10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000484 X transcript variant 1 NM_006013.3 NP_006004.2 78


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