The MAX gene homepage

General information
Gene symbol MAX
Gene name MYC associated factor X
Chromosome 14
Chromosomal band q23
Imprinted Unknown
Genomic reference NG_029830.1
Transcript reference NM_002382.4
Exon/intron information NM_002382.4 exon/intron table
Associated with diseases pheochromocytoma
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (2) Mercedes Robledo and Alberto Cascon
Total number of public variants reported 33
Unique public DNA variants reported 22
Individuals with public variants 21
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created July 20, 2011
Date last updated March 22, 2024
Version MAX:240322

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_002382.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.LOVD.nl/MAX
HGNC 6913
Entrez Gene 4149
PubMed articles MAX
OMIM - Gene 154950
OMIM - Diseases pheochromocytoma (pheochromocytoma (susceptibility to))
HGMD MAX
GeneCards MAX
GeneTests MAX
Orphanet MAX


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024166 14 transcript variant 1 NM_002382.4 NP_002373.3 33


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