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:3534 | Lafora disease | |
DOID:3535 | Unverricht-Lundborg syndrome | |
DOID:4090 | agnosia | |
DOID:4428 | dyslexia | |
DOID:4766 | embryoma | |
DOID:4964 | neurotic disorder | |
DOID:529 | blepharospasm | |
DOID:5418 | schizoaffective disorder | |
DOID:5419 | schizophrenia | |
DOID:5823 | childhood lymphoma |
HPO ID | HPO Term |
---|---|
HP:0001260 | Dysarthria |
HP:0001268 | Mental deterioration |
HP:0001288 | Gait disturbance |
HP:0001289 | Confusion |
HP:0001312 | Giant somatosensory evoked potentials |
HP:0001336 | Myoclonus |
HP:0001399 | Hepatic failure |
HP:0002069 | Bilateral tonic-clonic seizure |
HP:0002100 | Recurrent aspiration pneumonia |
HP:0002121 | Generalized non-motor (absence) seizure |
Disease ID | Disease Name |
---|---|
ORPHA:501 |
|
OMIM:254780 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100409236 | CALJA31805 | ||
105588793 | CERAT02590 | ||
699361 | MACMU34093 | ||
105488972 | MACNE10403 | ||
101007529 | PAPAN34746 | ||
748434 | PANTR39244 | ||
100450107 | PONAB31718 | ||
112919497 | VULVU11734 | ||
123797413 | URSAM23179 | ||
101096812 | FELCA10734 |
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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