1. Panels
  2. Intellectual_disability
  3. MAGEB2
Genes in panel
Prev Next
STRs in panel
Prev Next
Regions in panel
Prev Next

Intellectual_disability

Gene: MAGEB2

Red List (low evidence)
MAGEB2 (MAGE family member B2)
EnsemblGeneIds (GRCh38): ENSG00000099399
EnsemblGeneIds (GRCh37): ENSG00000099399
OMIM: 300098, Gene2Phenotype
MAGEB2 is in 1 panel

0 reviews

Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Candidate gene (Grozeva et al, 2015)
Phenotypes
  • Intellectual disability
OMIM
300098
Clinvar variants
Variants in MAGEB2
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

MAGEB2 was added to Intellectual_disabilitypanel. Sources: Candidate gene (Grozeva et al, 2015)