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:0002751 | Kyphoscoliosis |
HP:0002761 | Generalized joint hypermobility |
HP:0002827 | Hip dislocation |
HP:0003160 | Abnormal isoelectric focusing of serum transferrin |
HP:0003196 | Short nose |
HP:0003199 | Decreased muscle mass |
HP:0003429 | CNS hypomyelination |
HP:0003593 | Infantile onset |
HP:0003758 | Reduced subcutaneous adipose tissue |
HP:0004305 | Involuntary movements |
Disease ID | Disease Name |
---|---|
OMIM:617403 |
|
ORPHA:357074 |
|
OMIM:618012 |
|
ORPHA:442835 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
112151199 | ORYME19989 | |||
112913438 | VULVU04645 | |||
113029392 | ASTCA40869 | |||
113030837 | ASTCA01708 | |||
113163316 | ANATE01476 | |||
113444432 | PSETE17233 | |||
113477758 | ATHCN02273 | |||
113570270 | ELEEL07610 | |||
113576113 | ELEEL17708 | |||
113880466 | BOBOX29790 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024