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:0110111 | atrial heart septal defect 6 | |
DOID:0110112 | atrial heart septal defect 7 | |
DOID:0110113 | atrial heart septal defect 8 | |
DOID:0110114 | atrial heart septal defect 9 | |
DOID:0110213 | isolated cleft palate | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | |
DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C |
HPO ID | HPO Term |
---|---|
HP:0000541 | Retinal detachment |
HP:0000545 | Myopia |
HP:0000556 | Retinal dystrophy |
HP:0000557 | Buphthalmos |
HP:0000568 | Microphthalmia |
HP:0000587 | Abnormal optic nerve morphology |
HP:0000589 | Coloboma |
HP:0000609 | Optic nerve hypoplasia |
HP:0000612 | Iris coloboma |
HP:0000618 | Blindness |
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 |
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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