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  2. Intellectual_disability
  3. OGT
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Intellectual_disability

Gene: OGT

Red List (low evidence)
OGT (O-linked N-acetylglucosamine (GlcNAc) transferase)
EnsemblGeneIds (GRCh38): ENSG00000147162
EnsemblGeneIds (GRCh37): ENSG00000147162
OMIM: 300255, Gene2Phenotype
OGT is in 3 panels

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
300255
Clinvar variants
Variants in OGT
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

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