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STT3B

STT3 oligosaccharyltransferase complex catalytic subunit B

HCNC Approved Symbol
STT3B (HGNC:30611)
Genomic Coordinates
3:31,532,925 - 31,637,616 (3p23)
Synonyms
SIMP, FLJ90106, STT3-B
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 Ix
615597AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the STT3B gene.

Frequently observed phenotypes

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

No Results