LOVD TNFRSF10C homepage

General information
Gene name TNF receptor superfamily member 10c
Gene symbol TNFRSF10C
Chromosome Location 8p21.3
Database location Dalgleish Laboratory, Department of Genetics, University of Leicester, UK
Curator Zoe Baily, Marion MacFarlane and Raymond Dalgleish
PubMed references View all (unique) PubMed references in the TNFRSF10C database
Date of creation April 30, 2012
Last update January 21, 2015
Version TNFRSF10C150121
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_032578.1
Transcript refseq ID NM_003841.3
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 11
Total number of individuals with variant(s) 11
Total number of variants reported 11
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NOTE The work leading to the establishment of this LSDB was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 200754 - the GEN2PHEN project.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the TNFRSF10C 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 TNFRSF10C database, without patient data
Complete sequence variant listing Listing of all sequence variants in the TNFRSF10C database
Variants with no known pathogenicity Listing of all TNFRSF10C 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
Search through hidden entries Find the number of variant entries in the database (including hidden entries) matching your search terms.

Links to other resources
HGNC 11906
Entrez Gene 8794
OMIM - Gene 603613
UniProtKB (SwissProt/TrEMBL) O14798
GeneCards TNFRSF10C
GeneTests TNFRSF10C

Copyright & disclaimer
All contents of this database are protected by local and international copyright laws. The information is submitted for the purpose of sharing genetic and clinical information. Genetic variants listed may or may not have a causal association with disease phenotypes, irrespective of stated classifications or other information presented in the database. All information in this database, including variant classifications, is subject to change and there is no warranty, express or implied, as to its accuracy, completeness, or fitness for a particular purpose. Use of this database and information is subject to User responsibility and discretion. Clinical decisions regarding individual patient care should be carried out in conjunction with a healthcare professional with expertise in the relevant genes and diseases. We do not accept any liability for any injury, loss or damage incurred by use of or reliance on the information provided by this database.

Database submitters are required to adhere to their institution's rules for data sharing, and local and national laws. Personal identifiers should not be submitted. Submitters retain the rights to use and edit their data. Database curators may curate data to ensure that database formatting and quality standards are met. They may also share submitted data with external parties for research purposes or for sharing with other databases.