NOTE: the data displayed here derive from the NCL mutation and patient database - CLN7/MFSD8 and are shown only to link directly to their original source.
LOVD MFSD8 homepage

General information
Gene name Major facilitator superfamily domain containing 8
Gene symbol MFSD8
Chromosome Location 4q28.2
Database location grenada.lumc.nl
Curator LOVD-team, but with Curator vacancy and Sara Mole
Database reference for citations NCL Mutation and Patient Database
PubMed references View all (unique) PubMed references in the MFSD8 database
Date of creation April 29, 2010
Last update January 05, 2013
Version MFSD8 130105
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file coding DNA reference sequence for describing sequence variants
Genomic refseq ID NG_008657.1
Transcript refseq ID NM_152778.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 36
Total number of individuals with variant(s) 77
Total number of variants reported 150
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NOTE NOTE: the data displayed here derive from the NCL mutation and patient database - CLN7/MFSD8 and are shown only to link directly to their original source.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the MFSD8 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 MFSD8 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the MFSD8 database
Variants with no known pathogenicity Listing of all MFSD8 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
Homepage http://www.LOVD.nl/MFSD8
HGNC 28486
Entrez Gene 256471
OMIM - Gene 611124
OMIM - Disease ceroid lipofuscinosis,neuronal, type 7 (CLN-7)
UniProtKB (SwissProt/TrEMBL) Q8NHS3
HGMD MFSD8
GeneCards MFSD8
GeneTests MFSD8
External link #1 NCL mutation and patient database - CLN7/MFSD8
External link #2 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.

NOTE: the data displayed here derive from the NCL mutation and patient database - CLN7/MFSD8 and are shown only to link directly to their original source.