GO Term | Evidence Code | PMID |
---|---|---|
protein O-linked glycosylation | ||
nervous system development |
|
|
muscle organ development |
|
|
negative regulation of cell population proliferation | ||
regulation of protein glycosylation |
|
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
endoplasmic reticulum | ||
cis-Golgi network | ||
extracellular space |
|
|
Golgi apparatus |
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | XP_342839 | XM_342838 |
Caenorhabditis elegans | NP_497236 | NM_064835 |
Mus musculus | NP_647470 | NM_139309 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050428 | nonepidermolytic palmoplantar keratoderma | |
DOID:0050453 | lissencephaly | |
DOID:0050463 | campomelic dysplasia | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050700 | cardiomyopathy | |
DOID:0050777 | Joubert syndrome | |
DOID:0060249 | scoliosis |
HPO ID | HPO Term |
---|---|
HP:0003701 | Proximal muscle weakness |
HP:0003712 | Skeletal muscle hypertrophy |
HP:0003797 | Limb-girdle muscle atrophy |
HP:0004374 | Hemiplegia/hemiparesis |
HP:0006829 | Severe muscular hypotonia |
HP:0006888 | Meningoencephalocele |
HP:0007033 | Cerebellar dysplasia |
HP:0007126 | Proximal amyotrophy |
HP:0007260 | Type II lissencephaly |
HP:0007291 | Posterior fossa cyst |
Disease ID | Disease Name |
---|---|
ORPHA:370980 |
|
ORPHA:154 |
|
ORPHA:899 |
|
OMIM:613152 |
|
ORPHA:272 |
|
OMIM:236670 |
|
OMIM:253800 |
|
OMIM:611588 |
|
ORPHA:588 |
|
OMIM:611615 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115619890 | STRHB08052 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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