| Gene Symbol | STT3B |
| Entrez Gene ID | 201595 |
| Full Name | STT3B, catalytic subunit of the oligosaccharyltransferase complex |
| Synonyms | CDG1X,SIMP,STT3-B |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]. |
| Disorder MIM: | |
| Disorder Html: | ?Congenital disorder of glycosylation, type Ix, 615597 (3) |







































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