MAGEL2 gene homepage

General information
Gene symbol MAGEL2
Gene name MAGE-like 2
Chromosome 15
Chromosomal band q11-q12
Imprinted Imprinted, maternal
Genomic reference NG_016776.1
Transcript reference NM_019066.4
Exon/intron information NM_019066.4 exon/intron table
Associated with diseases autism, ID, SHFYNG
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Christian Schaaf
Total number of public variants reported 103
Unique public DNA variants reported 81
Individuals with public variants 12
Hidden variants 0
Date created May 03, 2013
Date last updated July 06, 2018
Version MAGEL2:180706

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_019066.4.
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
HGNC 6814
Entrez Gene 54551
PubMed articles MAGEL2
OMIM - Gene 605283
OMIM - Diseases autism
SHFYNG (Schaaf-Yang syndrome (SHFYNG))
GeneCards MAGEL2
GeneTests MAGEL2

Active transcripts




NCBI ID     

NCBI Protein ID     

00011687 15 MAGE-like 2 NM_019066.4 NP_061939.3 103

Copyright & disclaimer
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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.