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MGAT2

alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase

HCNC Approved Symbol
MGAT2 (HGNC:7045)
Genomic Coordinates
14:49,620,799 - 49,623,481 (14q21.3)
Synonyms
GNT-II
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Congenital disorder of glycosylation, type IIa
212066AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MGAT2 gene.

Frequently observed phenotypes

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

No Results