LOVD RPL11 homepage

General information
Gene name ribosomal protein L11
Gene symbol RPL11
Chromosome Location 1p36.1-p35
Database location www.dbagenes.unito.it
Curator I. Boria and U. Ramenghi
Database reference for citations The ribosomal basis of diamond-blackfan anemia: mutation and database update. Boria et al (2010) Hum Mutat [Epub ahead of print]
PubMed references View all (unique) PubMed references in the RPL11 database
Date of creation June 11, 2010
Last update November 19, 2010
Version RPL11 101119
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Reference sequence file coding DNA reference sequence for describing sequence variants
Genomic refseq ID NC_000001.10
Transcript refseq ID NM_000975.2
Total number of unique DNA variants reported 26
Total number of individuals with variant(s) 37
Total number of variants reported 37
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NOTE The RPL11 gene comprises 6 exons and spans 4.6 kb. The predicted size of the primary transcript is 609 bp; it encodes for a 178 amino acid protein (MW 20.1 kDa).
Link to the location of the pathogenic variants in relation to the gene

This database was partially supported by the ENERCA (European Network for Rare and Congenital Anaemias) project.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the RPL11 database, sorted by type of variant (with graphical displays and statistics)
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the RPL11 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the RPL11 database
Variants with no known pathogenicity Listing of all RPL11 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
HGNC 10301
Entrez Gene 6135
OMIM - Gene 604175
OMIM - Disease 612562 (DBA7)
UniProtKB (SwissProt/TrEMBL) P62913
External link dbSNP

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2018. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.