UniProt | Protein Name |
---|---|
Q06210 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein N-linked glycosylation | ||
circadian regulation of gene expression | ||
glutamine metabolic process | ||
energy reserve metabolic process |
|
|
UDP-N-acetylglucosamine biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol |
|
|
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
carbohydrate derivative binding | ||
glutamine-fructose-6-phosphate transaminase (isomerizing) activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050782 | Zollinger-Ellison syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080089 | tubular aggregate myopathy 1 | |
DOID:0110660 | congenital myasthenic syndrome 12 | |
DOID:0110679 | congenital myasthenic syndrome 4C |
HPO ID | HPO Term |
---|---|
HP:0002355 | Difficulty walking |
HP:0002359 | Frequent falls |
HP:0002421 | Poor head control |
HP:0002460 | Distal muscle weakness |
HP:0002515 | Waddling gait |
HP:0002650 | Scoliosis |
HP:0002747 | Respiratory insufficiency due to muscle weakness |
HP:0002804 | Arthrogryposis multiplex congenita |
HP:0002938 | Lumbar hyperlordosis |
HP:0003198 | Myopathy |
Disease ID | Disease Name |
---|---|
OMIM:610542 |
|
OMIM:608931 |
|
ORPHA:353327 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102457021 | PELSI05392 | ||
114045306 | VOMUR04812 | ||
113901396 | BOBOX18708 | ||
100955987 | OTOGA09026 | ||
101071849 | TAKRU29706 | ||
102025483 | CHILA07757 | ||
105704615 | AOTNA37799 | ||
110207645 | PHACI23847 | ||
101053058 | SAIBB04860 | ||
101611596 | JACJA13534 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024