UniProt | Protein Name |
---|---|
O95278 |
|
GO Term | Evidence Code | PMID |
---|---|---|
regulation of proteasomal protein catabolic process |
|
|
regulation of cell growth |
|
|
autophagosome assembly |
|
|
protein dephosphorylation |
|
|
negative regulation of dephosphorylation |
|
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:0050776 | non-syndromic X-linked intellectual disability | |
DOID:0050841 | focal hand dystonia | |
DOID:0060058 | lymphoma | |
DOID:0060135 | apraxia | |
DOID:0060162 | dentatorubral-pallidoluysian atrophy | |
DOID:0060171 | obsolete Dravet syndrome | |
DOID:0060215 | Balo concentric sclerosis | |
DOID:0060281 | photosensitive epilepsy | |
DOID:0080422 | Dravet syndrome | |
DOID:0110720 | neuronal ceroid lipofuscinosis 4 |
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