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:0001260 | Dysarthria |
HP:0001270 | Motor delay |
HP:0001284 | Areflexia |
HP:0001290 | Generalized hypotonia |
HP:0001371 | Flexion contracture |
HP:0001382 | Joint hypermobility |
HP:0001558 | Decreased fetal movement |
HP:0001612 | Weak cry |
HP:0001763 | Pes planus |
HP:0002015 | Dysphagia |
Disease ID | Disease Name |
---|---|
OMIM:610542 |
|
OMIM:608931 |
|
ORPHA:353327 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102443324 | MYOLU07720 | ||
117033189 | RHIFE24953 | ||
100229923 | TAEGU13181 | ||
101811675 | FICAL12338 | ||
103220112 | CHLSB04244 | ||
108516326 | RHIBE22306 | ||
104665730 | RHIRO27452 | ||
100599112 | NOMLE08446 | ||
114602667 | PODMU32103 | ||
106828330 | EQUAS19167 |
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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