UniProt | Protein Name |
---|---|
Q9Y487 |
|
GO Term | Evidence Code | PMID |
---|---|---|
Golgi lumen acidification |
|
|
regulation of macroautophagy |
|
|
immune response |
|
|
intracellular iron ion homeostasis | ||
vacuolar acidification |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
vacuolar proton-transporting V-type ATPase, V0 domain | ||
proton-transporting V-type ATPase complex |
|
|
transmembrane transporter complex | ||
plasma membrane |
GO Term | Evidence Code | PMID |
---|---|---|
ATPase binding | ||
proton-transporting ATPase activity, rotational mechanism | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:12531 | von Willebrand's disease | |
DOID:1307 | dementia | |
DOID:13328 | diabetic cataract | |
DOID:13359 | Ehlers-Danlos syndrome | |
DOID:13533 | osteopetrosis | |
DOID:14219 | renal tubular acidosis | |
DOID:1612 | breast cancer | |
DOID:162 | cancer | |
DOID:1712 | aortic valve stenosis | |
DOID:1824 | status epilepticus |
HPO ID | HPO Term |
---|---|
HP:0002751 | Kyphoscoliosis |
HP:0002761 | Generalized joint hypermobility |
HP:0002808 | Kyphosis |
HP:0002812 | Coxa vara |
HP:0003100 | Slender long bone |
HP:0003160 | Abnormal isoelectric focusing of serum transferrin |
HP:0003196 | Short nose |
HP:0003199 | Decreased muscle mass |
HP:0003577 | Congenital onset |
HP:0003691 | Scapular winging |
Disease ID | Disease Name |
---|---|
OMIM:219200 |
|
ORPHA:357074 |
|
OMIM:278250 |
|
ORPHA:2834 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109061555 | CYPCA137069 | ||
109100783 | CYPCA14959 | ||
103739020 | NANGA07936 | ||
116452945 | CORMO06544 | ||
103259682 | CARSF19588 | ||
115614949 | STRHB19967 |
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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