The MAGEL2 gene homepage

General information
Gene symbol MAGEL2
Gene name MAGE-like 2
Chromosome 15
Chromosomal band q11-q12
Imprinted Unknown
Genomic reference NG_016776.1
Transcript reference NM_019066.4
Associated with diseases autism, ID, SHFYNG
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 7
Unique public DNA variants reported 2
Individuals with public variants 7
Hidden variants -
Date created November 30, -0001
Date last updated September 28, 2016
Version MAGEL2:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:6814
Entrez Gene 54551
PubMed articles MAGEL2
OMIM - Gene 605283
OMIM - Diseases autism
SHFYNG (Schaaf-Yang syndrome (SHFYNG))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00028551 15 MAGE-like 2 NM_019066.4 NP_061939.3 7