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:8577 | ulcerative colitis | |
DOID:8778 | Crohn's disease | |
DOID:8927 | learning disability | |
DOID:8947 | diabetic retinopathy | |
DOID:9306 | mechanical strabismus | |
DOID:9521 | Laron syndrome | |
DOID:9588 | encephalitis | |
DOID:9675 | pulmonary emphysema | |
DOID:9837 | hypertropia | |
DOID:987 | alopecia |
HPO ID | HPO Term |
---|---|
HP:0002097 | Emphysema |
HP:0002126 | Polymicrogyria |
HP:0002133 | Status epilepticus |
HP:0002187 | Intellectual disability, profound |
HP:0002208 | Coarse hair |
HP:0002299 | Brittle hair |
HP:0002361 | Psychomotor deterioration |
HP:0002465 | Poor speech |
HP:0002645 | Wormian bones |
HP:0002650 | Scoliosis |
Disease ID | Disease Name |
---|---|
OMIM:219200 |
|
ORPHA:357074 |
|
OMIM:278250 |
|
ORPHA:2834 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101076155 | TAKRU29466 | ||
102026867 | CHILA18414 | ||
110196835 | PHACI21044 | ||
108435410 | PYGNA19368 | ||
101971514 | ICTTR06584 | ||
118285461 | SCOMX09523 | ||
118314112 | SCOMX32825 | ||
102434782 | MYOLU16890 | ||
100218036 | TAEGU05934 | ||
101806637 | FICAL01983 |
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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