LOVD TMEM237 homepage

General information
Gene name Transmembrane protein 237
Gene symbol TMEM237
Chromosome Location 2q33
Database location http://grenada.lumc.nl/LOVD2/shared1
Curator Lijia Huang
PubMed references View all (unique) PubMed references in the TMEM237 database
Date of creation January 31, 2012
Last update June 25, 2013
Version TMEM237 130625
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_032049.1
Transcript refseq ID NM_001044385.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 6
Total number of individuals with variant(s) 20
Total number of variants reported 40
Subscribe to updates of this gene
NOTE The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the TMEM237 database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
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 TMEM237 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the TMEM237 database
Variants with no known pathogenicity Listing of all TMEM237 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)
Download table Download the full sequence variant table of the TMEM237 database in tab-delimited text format.

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
Homepage http://www.LOVD.nl/TMEM237
HGNC 14432
Entrez Gene 65062
OMIM - Gene 614423
OMIM - Disease Joubert syndrome, type 14 (JBTS-14)
UniProtKB (SwissProt/TrEMBL) Q96Q45
GeneCards TMEM237
External link Orphanet

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 © 2016. 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.