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 |
---|---|---|
proton-transporting V-type ATPase complex |
|
|
transmembrane transporter complex | ||
plasma membrane | ||
vacuolar proton-transporting V-type ATPase, V1 domain | ||
membrane |
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:4090 | agnosia | |
DOID:0050133 | superficial mycosis | |
DOID:0050453 | lissencephaly | |
DOID:0050591 | tooth agenesis | |
DOID:0050700 | cardiomyopathy | |
DOID:0050777 | Joubert syndrome | |
DOID:0050841 | focal hand dystonia | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060270 | pontocerebellar hypoplasia type 2D |
HPO ID | HPO Term |
---|---|
HP:0001511 | Intrauterine growth retardation |
HP:0001519 | Disproportionate tall stature |
HP:0001558 | Decreased fetal movement |
HP:0001582 | Redundant skin |
HP:0001631 | Atrial septal defect |
HP:0001635 | Congestive heart failure |
HP:0001639 | Hypertrophic cardiomyopathy |
HP:0001762 | Talipes equinovarus |
HP:0002020 | Gastroesophageal reflux |
HP:0002059 | Cerebral atrophy |
Disease ID | Disease Name |
---|---|
OMIM:618012 |
|
ORPHA:357074 |
|
ORPHA:442835 |
|
OMIM:617403 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102298187 | HAPBU08336 | ||
102305101 | HAPBU00615 | ||
113029392 | ASTCA40869 | ||
113030837 | ASTCA01708 | ||
115570340 | SPAAU46662 | ||
115594565 | SPAAU18916 | ||
734627 | Xenbase:XB-GENE-865279 | ||
108709283 | Xenbase:XB-GENE-17340515 | ||
407846 | Xenbase:XB-GENE-990439 | ||
493238 | Xenbase:XB-GENE-479548 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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