UniProt | Protein Name |
---|---|
P38606 |
|
GO Term | Evidence Code | PMID |
---|---|---|
intracellular iron ion homeostasis | ||
synaptic vesicle lumen acidification | ||
endosomal lumen acidification | ||
intracellular pH reduction | ||
proton motive force-driven ATP synthesis |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
plasma membrane | ||
nucleoplasm | ||
clathrin-coated vesicle membrane | ||
extrinsic component of synaptic vesicle membrane |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
ATP hydrolysis activity | ||
proton-transporting ATPase activity, rotational mechanism | ||
proton-transporting ATP synthase activity, rotational mechanism | ||
ATP binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0070129 | autosomal recessive cutis laxa type IID | |
DOID:0112275 | developmental and epileptic encephalopathy 93 |
HPO ID | HPO Term |
---|---|
HP:0002317 | Unsteady gait |
HP:0002355 | Difficulty walking |
HP:0002361 | Psychomotor deterioration |
HP:0002373 | Febrile seizure (within the age range of 3 months to 6 years) |
HP:0002376 | Developmental regression |
HP:0002421 | Poor head control |
HP:0002465 | Poor speech |
HP:0002509 | Limb hypertonia |
HP:0002521 | Hypsarrhythmia |
HP:0002540 | Inability to walk |
Disease ID | Disease Name |
---|---|
OMIM:617403 |
|
ORPHA:357074 |
|
OMIM:618012 |
|
ORPHA:442835 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
109058575 | CYPCA130418 | |||
109089969 | CYPCA14994 | |||
109319171 | CROPO06169 | |||
109514041 | HIPCM25504 | |||
109517920 | HIPCM09392 | |||
110222274 | PHACI00680 | |||
111221014 | SERDU21131 | |||
111234447 | SERDU12801 | |||
111587180 | AMPOC11867 | |||
112142898 | ORYME12285 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024