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:422 | congenital structural myopathy | |
DOID:423 | myopathy | |
DOID:439 | neuromuscular junction disease | |
DOID:440 | neuromuscular disease | |
DOID:4480 | achondroplasia | |
DOID:4766 | embryoma | |
DOID:4905 | pancreatic carcinoma | |
DOID:539 | ophthalmoplegia | |
DOID:540 | strabismus | |
DOID:5517 | stomach carcinoma |
HPO ID | HPO Term |
---|---|
HP:0003199 | Decreased muscle mass |
HP:0003200 | Ragged-red muscle fibers |
HP:0003202 | Skeletal muscle atrophy |
HP:0003236 | Elevated circulating creatine kinase concentration |
HP:0003325 | Limb-girdle muscle weakness |
HP:0003388 | Easy fatigability |
HP:0003391 | Gowers sign |
HP:0003394 | Muscle spasm |
HP:0003403 | EMG: decremental response of compound muscle action potential to repetitive nerve stimulation |
HP:0003443 | Decreased size of nerve terminals |
Disease ID | Disease Name |
---|---|
OMIM:610542 |
|
OMIM:608931 |
|
ORPHA:353327 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115618382 | STRHB19566 |
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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