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 |
---|---|---|
plasma membrane |
|
|
nucleoplasm |
|
|
perikaryon |
|
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:1059 | intellectual disability | |
DOID:10652 | Alzheimer's disease | |
DOID:11328 | schizophreniform disorder | |
DOID:1206 | Rett syndrome | |
DOID:12139 | dysthymic disorder | |
DOID:1289 | neurodegenerative disease | |
DOID:1307 | dementia | |
DOID:13417 | alexia | |
DOID:1432 | blindness | |
DOID:1443 | cerebral degeneration |
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 |
---|---|---|---|
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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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