UniProt | Protein Name |
---|---|
P98160 |
|
GO Term | Evidence Code | PMID |
---|---|---|
animal organ regeneration | ||
brain development |
|
|
response to xenobiotic stimulus | ||
angiogenesis | ||
positive regulation of endothelial cell proliferation |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular region | ||
Golgi lumen |
|
|
basement membrane |
|
|
plasma membrane |
|
|
focal adhesion |
GO Term | Evidence Code | PMID |
---|---|---|
low-density lipoprotein particle receptor binding |
|
|
amyloid-beta binding | ||
extracellular matrix structural constituent conferring compression resistance | ||
calcium ion binding | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:1156 | chondrocalcinosis | |
DOID:1168 | familial hyperlipidemia | |
DOID:11714 | gestational diabetes | |
DOID:11719 | oculopharyngeal muscular dystrophy | |
DOID:11720 | distal myopathy | |
DOID:11722 | myotonic dystrophy type 1 | |
DOID:11723 | Duchenne muscular dystrophy | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:11725 | Cornelia de Lange syndrome | |
DOID:11727 | facioscapulohumeral muscular dystrophy |
HPO ID | HPO Term |
---|---|
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001265 | Hyporeflexia |
HP:0001274 | Agenesis of corpus callosum |
HP:0001276 | Hypertonia |
HP:0001288 | Gait disturbance |
HP:0001324 | Muscle weakness |
HP:0001344 | Absent speech |
HP:0001362 | Calvarial skull defect |
HP:0001371 | Flexion contracture |
Disease ID | Disease Name |
---|---|
ORPHA:1606 |
|
ORPHA:800 |
|
ORPHA:1865 |
|
OMIM:255800 |
|
OMIM:224410 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
403440 | CANLF07063 | ||
100467831 | AILME12467 | ||
101681560 | MUSPF18500 | ||
101094520 | FELCA19382 | ||
122226287 | PANLE10175 | ||
118890557 | BALMU22335 | ||
100071701 | HORSE27583 | ||
100517288 | PIGXX29237 | ||
444872 | BOVIN25243 | ||
102188640 | CAPHI19907 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024