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:0003473 | Fatigable weakness |
HP:0003551 | Difficulty climbing stairs |
HP:0003554 | Type 2 muscle fiber atrophy |
HP:0003593 | Infantile onset |
HP:0003621 | Juvenile onset |
HP:0003623 | Neonatal onset |
HP:0003680 | Nonprogressive |
HP:0003691 | Scapular winging |
HP:0003701 | Proximal muscle weakness |
HP:0003803 | Type 1 muscle fiber predominance |
Disease ID | Disease Name |
---|---|
OMIM:610542 |
|
OMIM:608931 |
|
ORPHA:353327 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115164533 | SALTR60789 | ||
115200115 | SALTR22879 | ||
115545397 | GADMO52473 | ||
101170101 | ORYLA17744 | ||
115581277 | SPAAU13257 | ||
414702 | Xenbase:XB-GENE-866299 | ||
100485575 | Xenbase:XB-GENE-493902 | ||
100490693 | Xenbase:XB-GENE-948420 | ||
101936574 | CHRPI07606 | ||
109317328 | CROPO24852 |
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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