UniProt | Protein Name |
---|---|
O95278 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of TOR signaling | ||
negative regulation of peptidyl-serine phosphorylation |
|
|
regulation of protein localization to plasma membrane |
|
|
proteasome-mediated ubiquitin-dependent protein catabolic process |
|
|
calcium ion transport |
|
GO Term | Evidence Code | PMID |
---|---|---|
phosphatase activity |
|
|
glycogen (starch) synthase activity |
|
|
starch binding |
|
|
protein serine/threonine phosphatase activity |
|
|
protein homodimerization activity |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:14503 | neuronal ceroid lipofuscinosis | |
DOID:1470 | major depressive disorder | |
DOID:1595 | melancholic depression | |
DOID:1596 | depressive disorder | |
DOID:162 | cancer | |
DOID:1824 | status epilepticus | |
DOID:1826 | epilepsy | |
DOID:2468 | psychotic disorder | |
DOID:2481 | obsolete infantile epileptic encephalopathy | |
DOID:2747 | glycogen storage disease |
HPO ID | HPO Term |
---|---|
HP:0002123 | Generalized myoclonic seizure |
HP:0002133 | Status epilepticus |
HP:0002186 | Apraxia |
HP:0002315 | Headache |
HP:0002344 | Progressive neurologic deterioration |
HP:0002360 | Sleep abnormality |
HP:0002367 | Visual hallucination |
HP:0002384 | Focal impaired awareness seizure |
HP:0002521 | Hypsarrhythmia |
HP:0002540 | Inability to walk |
Disease ID | Disease Name |
---|---|
ORPHA:501 |
|
OMIM:254780 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
113898510 | BOBOX27299 | ||
101064710 | TAKRU15327 | ||
102798438 | NEOBR12379 | ||
108240062 | KRYMA15426 | ||
105717564 | AOTNA05345 | ||
111235445 | SERDU01872 | ||
103134907 | POEFO00364 | ||
117016579 | RHIFE11332 | ||
100223137 | TAEGU20894 | ||
103240208 | CHLSB03629 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024