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 |
---|---|---|
myosin phosphatase activity |
|
|
protein tyrosine/serine/threonine phosphatase activity |
|
|
protein tyrosine phosphatase activity |
|
|
carbohydrate binding |
|
|
carbohydrate phosphatase activity |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:2749 | glycogen storage disease Ia | |
DOID:2848 | obsolete melancholia | |
DOID:2862 | glucosephosphate dehydrogenase deficiency | |
DOID:2871 | endometrial carcinoma | |
DOID:308 | early myoclonic encephalopathy | |
DOID:310 | MERRF syndrome | |
DOID:3159 | photosensitivity disease | |
DOID:3234 | central nervous system lymphoma | |
DOID:331 | central nervous system disease | |
DOID:3329 | benign epilepsy with centrotemporal spikes |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000572 | Visual loss |
HP:0000709 | Psychosis |
HP:0000712 | Emotional lability |
HP:0000716 | Depression |
HP:0000726 | Dementia |
HP:0000992 | Cutaneous photosensitivity |
HP:0001250 | Seizure |
HP:0001251 | Ataxia |
HP:0001257 | Spasticity |
Disease ID | Disease Name |
---|---|
ORPHA:501 |
|
OMIM:254780 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109080985 | CYPCA115813 | ||
116440858 | CORMO18012 | ||
115613561 | STRHB13439 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024