LOVD MAX homepage

General information
Gene name MYC associated factor X
Gene symbol MAX
Chromosome Location 14q23
Database location http://grenada.lumc.nl/LOVD2/shared1
Curator LOVD-team, but with Curator vacancy
PubMed references View all (unique) PubMed references in the MAX database
Date of creation July 20, 2011
Last update August 31, 2011
Version MAX110831
Add sequence variant Submit a sequence variant
First time submitters Register here
Genomic refseq ID NG_029830.1
Transcript refseq ID NM_002382.3
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 8
Total number of individuals with variant(s) 12
Total number of variants reported 12
Subscribe to updates of this gene

Graphical displays and utilities
Summary tables Summary of all sequence variants in the MAX 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 MAX database, without patient data
Complete sequence variant listing Listing of all sequence variants in the MAX database
Variants with no known pathogenicity Listing of all MAX 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 6913
Entrez Gene 4149
OMIM - Gene 154950
UniProtKB (SwissProt/TrEMBL) P61244
GeneCards MAX
GeneTests MAX
External link Orphanet