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 |
---|---|---|---|---|
101972279 | ICTTR13734 | |||
102003528 | CHILA03576 | |||
102135340 | MACFA10681 | |||
102184597 | CAPHI19154 | |||
102437127 | MYOLU13436 | |||
102450612 | PELSI04393 | |||
102526127 | VICPA07745 | |||
103035415 | ASTMX02969 | |||
103180290 | CALMI20061 | |||
103248767 | CHLSB01151 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024