UniProt | Protein Name |
---|---|
P38606 |
|
GO Term | Evidence Code | PMID |
---|---|---|
proton motive force-driven ATP synthesis | ||
Golgi lumen acidification |
|
|
synaptic vesicle lumen acidification | ||
regulation of macroautophagy |
|
|
intracellular pH reduction |
|
GO Term | Evidence Code | PMID |
---|---|---|
extrinsic component of synaptic vesicle membrane | ||
intracellular membrane-bounded organelle | ||
cytosol | ||
clathrin-coated vesicle membrane | ||
secretory granule |
GO Term | Evidence Code | PMID |
---|---|---|
proton-transporting ATPase activity, rotational mechanism | ||
proton-transporting ATP synthase activity, rotational mechanism | ||
ATP binding | ||
protein binding | ||
ATP hydrolysis activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:1731 | histoplasmosis | |
DOID:1759 | American histoplasmosis | |
DOID:1824 | status epilepticus | |
DOID:1826 | epilepsy | |
DOID:1882 | atrial heart septal defect | |
DOID:216 | dental caries | |
DOID:2481 | obsolete infantile epileptic encephalopathy | |
DOID:2725 | capillary hemangioma | |
DOID:2785 | Dandy-Walker syndrome | |
DOID:308 | early myoclonic encephalopathy |
HPO ID | HPO Term |
---|---|
HP:0002063 | Rigidity |
HP:0002069 | Bilateral tonic-clonic seizure |
HP:0002079 | Hypoplasia of the corpus callosum |
HP:0002097 | Emphysema |
HP:0002107 | Pneumothorax |
HP:0002126 | Polymicrogyria |
HP:0002133 | Status epilepticus |
HP:0002171 | Gliosis |
HP:0002187 | Intellectual disability, profound |
HP:0002208 | Coarse hair |
Disease ID | Disease Name |
---|---|
OMIM:618012 |
|
ORPHA:357074 |
|
ORPHA:442835 |
|
OMIM:617403 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103257766 | CARSF17799 | ||
115601664 | STRHB05004 |
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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