UniProt | Protein Name |
---|---|
Q75T13 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of ER to Golgi vesicle-mediated transport | ||
embryonic pattern specification | ||
sensory perception of sound | ||
GPI anchor metabolic process | ||
anterior/posterior axis specification |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol deacylase activity | ||
hydrolase activity, acting on ester bonds |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:1443 | cerebral degeneration | |
DOID:1470 | major depressive disorder | |
DOID:1595 | melancholic depression | |
DOID:1596 | depressive disorder | |
DOID:1826 | epilepsy | |
DOID:2231 | factor XII deficiency | |
DOID:2234 | focal epilepsy | |
DOID:2303 | stereotypic movement disorder | |
DOID:2481 | obsolete infantile epileptic encephalopathy | |
DOID:2848 | obsolete melancholia |
HPO ID | HPO Term |
---|---|
HP:0001642 | Pulmonic stenosis |
HP:0001684 | Secundum atrial septal defect |
HP:0002059 | Cerebral atrophy |
HP:0002061 | Lower limb spasticity |
HP:0002064 | Spastic gait |
HP:0002069 | Bilateral tonic-clonic seizure |
HP:0002079 | Hypoplasia of the corpus callosum |
HP:0002120 | Cerebral cortical atrophy |
HP:0002121 | Generalized non-motor (absence) seizure |
HP:0002162 | Low posterior hairline |
Disease ID | Disease Name |
---|---|
OMIM:615802 |
|
ORPHA:401820 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
113007935 | ASTCA13198 | ||
115587832 | SPAAU27955 | ||
447534 | Xenbase:XB-GENE-5818693 | ||
101946941 | CHRPI22636 | ||
105579987 | CERAT00374 | ||
102139883 | MACFA05666 | ||
696475 | MACMU05679 | ||
105468162 | MACNE08816 | ||
101018135 | PAPAN01368 | ||
105551792 | MANLE26474 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024