MAGEL2
From SNPedia
is a | gene |
is | mentioned by |
Full name | MAGE family member L2 |
EntrezGene | 54551 |
PheGenI | 54551 |
VariationViewer | 54551 |
ClinVar | MAGEL2 |
GeneCards | MAGEL2 |
dbSNP | 54551 |
Diseases | MAGEL2 |
SADR | 54551 |
HugeNav | 54551 |
wikipedia | MAGEL2 |
MAGEL2 | |
gopubmed | MAGEL2 |
EVS | MAGEL2 |
HEFalMp | MAGEL2 |
MyGene2 | MAGEL2 |
23andMe | MAGEL2 |
Ensembl | ENSG00000254585 |
OMIM | 605283 |
# SNPs | 12 |
Max Magnitude | Chromosome position | Summary | |
---|---|---|---|
rs1060499934 | 0 | 23,644,785 | |
rs398122415 | 9 | 23,646,091 | |
rs398122416 | 9 | 23,645,941 | |
rs398122417 | 9 | 23,644,561 | |
rs398122418 | 9 | 23,644,619 | |
rs752097874 | 0 | 23,645,747 | |
rs770374710 | 9 | 23,645,746 | |
rs773586710 | 0 | 23,645,747 | |
rs797044883 | 0 | 23,645,831 | |
rs869312694 | 0 | 23,644,535 | |
rs886041598 | 0 | 23,645,580 | |
rs886041955 | 0 | 23,645,672 |
The MAGEL2 gene on chromosome 15 encodes a ubiquitin ligase enhancer. MAGEL2 is one of the paternally expressed genes within the Prader-Willi syndrome (PWS) locus, and mutations in MAGEL2 have been reported in individuals with features resembling PWS, called Schaaf-Yang syndrome.OMIM