UniProt | Protein Name |
---|---|
O95278 |
|
GO Term | Evidence Code | PMID |
---|---|---|
regulation of protein ubiquitination |
|
|
negative regulation of phosphatase activity |
|
|
L-glutamate transmembrane transport |
|
|
dephosphorylation |
|
|
Wnt signaling pathway |
|
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:0003678 | Rapidly progressive |
HP:0007270 | Atypical absence seizure |
HP:0007334 | Bilateral tonic-clonic seizure with focal onset |
HP:0007359 | Focal-onset seizure |
HP:0007537 | Severe photosensitivity |
HP:0010819 | Atonic seizure |
HP:0011165 | Focal sensory seizure with visual features |
HP:0012444 | Brain atrophy |
HP:0100318 | Lafora bodies |
Disease ID | Disease Name |
---|---|
ORPHA:501 |
|
OMIM:254780 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
122220465 | PANLE16311 | ||
118905237 | BALMU27021 | ||
100659008 | LOXAF20497 | ||
526888 | BOVIN35929 | ||
105993631 | DIPOR13175 | ||
13853 | MGI:1341085 | MOUSE01898 | |
114005 | RGD:71047 | RATNO17040 | |
100731363 | CAVPO19127 | ||
101563212 | OCTDE05991 | ||
107086044 | CYPVA08819 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024