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 |
---|---|---|
Golgi membrane |
|
|
endosome membrane |
|
|
nucleoplasm |
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:1307 | dementia | |
DOID:13174 | dissociated nystagmus | |
DOID:13450 | coccidioidomycosis | |
DOID:13564 | aspergillosis | |
DOID:13620 | patent foramen ovale | |
DOID:13714 | anodontia | |
DOID:13902 | white piedra | |
DOID:13976 | peptic esophagitis | |
DOID:1443 | cerebral degeneration | |
DOID:14484 | sporotrichosis |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000054 | Micropenis |
HP:0000218 | High palate |
HP:0000252 | Microcephaly |
HP:0000253 | Progressive microcephaly |
HP:0000272 | Malar flattening |
HP:0000278 | Retrognathia |
HP:0000298 | Mask-like facies |
Disease ID | Disease Name |
---|---|
OMIM:618012 |
|
ORPHA:357074 |
|
ORPHA:442835 |
|
OMIM:617403 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101693688 | MUSPF09648 | ||
101091723 | FELCA22962 | ||
101336142 | TURTR02445 | ||
118894824 | BALMU18312 | ||
100653567 | LOXAF11247 | ||
100061223 | HORSE14466 | ||
445531 | PIGXX05670 | ||
282147 | BOVIN14516 | ||
102186053 | CAPHI11869 | ||
101102025 | SHEEP01381 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024