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: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:617403 |
|
ORPHA:357074 |
|
OMIM:618012 |
|
ORPHA:442835 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
101819794 | FICAL09781 | |||
101878270 | MELUD18091 | |||
101943757 | CHRPI31880 | |||
101969020 | ICTTR00976 | |||
102005949 | CHILA08381 | |||
102186053 | CAPHI11869 | |||
102221550 | XIPMA19516 | |||
102233759 | XIPMA02933 | |||
102298187 | HAPBU08336 | |||
102305101 | HAPBU00615 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024