UniProt | Protein Name |
---|---|
P46977 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein N-linked glycosylation | ||
protein N-linked glycosylation via asparagine | ||
post-translational protein modification | ||
co-translational protein modification |
GO Term | Evidence Code | PMID |
---|---|---|
dolichyl-diphosphooligosaccharide-protein glycotransferase activity | ||
metal ion binding | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:11832 | visual epilepsy | |
DOID:0050570 | congenital disorder of glycosylation type I | |
DOID:0080572 | congenital disorder of glycosylation Iw | |
DOID:10112 | sleeping sickness | |
DOID:10113 | trypanosomiasis | |
DOID:10907 | microcephaly | |
DOID:1094 | attention deficit hyperactivity disorder | |
DOID:13777 | epidermodysplasia verruciformis | |
DOID:1470 | major depressive disorder | |
DOID:1520 | colon carcinoma |
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:619714 |
|
OMIM:615596 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100174363 | PONAB04013 | ||
123792710 | URSAM18079 | ||
100467601 | AILME07921 | ||
101685869 | MUSPF14638 | ||
101083108 | FELCA24655 | ||
118899285 | BALMU08071 | ||
100658795 | LOXAF07060 | ||
100064353 | HORSE40073 | ||
100072333 | HORSE40073 | ||
100511525 | PIGXX35731 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024