UniProt | Protein Name |
---|---|
P46977 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein N-linked glycosylation via asparagine | ||
protein N-linked glycosylation | ||
co-translational protein modification | ||
post-translational protein modification |
InterPro |
---|
Oligosaccharyl transferase STT3, N-terminal domain |
Oligosaccharyl transferase, STT3 subunit |
STT3/PglB/AglB, core domain |
DO ID | Disease Name | Source |
---|---|---|
DOID:0080572 | congenital disorder of glycosylation Iw |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000028 | Cryptorchidism |
HP:0000046 | Small scrotum |
HP:0000054 | Micropenis |
HP:0000219 | Thin upper lip vermilion |
HP:0000252 | Microcephaly |
HP:0000256 | Macrocephaly |
HP:0000276 | Long face |
HP:0000303 | Mandibular prognathia |
Disease ID | Disease Name |
---|---|
ORPHA:370921 |
|
OMIM:615596 |
|
OMIM:619714 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
101083108 | FELCA24655 | |||
101110978 | SHEEP10933 | |||
101133351 | 9595_0:0033db | GORGO03556 | ||
101577371 | OCTDE19997 | |||
101685869 | MUSPF14638 | |||
101700446 | HETGA18169 | |||
101815558 | FICAL07297 | |||
101869743 | MELUD17548 | |||
101933331 | CHRPI14970 | |||
101968095 | ICTTR13734 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024