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STT3A

STT3 oligosaccharyltransferase complex catalytic subunit A

HCNC Approved Symbol
STT3A (HGNC:6172)
Genomic Coordinates
11:125,591,769 - 125,623,091 (11q24.2)
Synonyms
TMC, MGC9042, STT3-A, ITM1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Congenital disorder of glycosylation, type Iw, autosomal dominant
619714AD
Congenital disorder of glycosylation, type Iw, autosomal recessive
615596AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the STT3A gene.

Frequently observed phenotypes

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

No Results