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: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 |
---|---|---|---|
100700921 | ORENI19149 | ||
102313696 | HAPBU02123 | ||
113006867 | ASTCA10530 | ||
115574001 | SPAAU62320 | ||
444115 | Xenbase:XB-GENE-965656 | ||
100170449 | Xenbase:XB-GENE-965638 | ||
101939759 | CHRPI34328 | ||
109320144 | CROPO06062 | ||
103818456 | SERCA13957 | ||
100075437 | ORNAN16839 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024