OGT - Gene browser | 3billion

OGT

OGT

O-linked N-acetylglucosamine (GlcNAc) transferase

HCNC Approved Symbol: OGT (HGNC:8127)
Genomic Coordinates: 23:71,533,104 - 71,575,892 (Xq13.1)
Synonyms: O-GLCNAC, HRNT1, MGC22921, FLJ23071, OGT1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the OGT gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

01
Patient count

Macrocephaly: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Seizure: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

OGT - Gene browser | 3billion