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:0090132 | complex cortical dysplasia with other brain malformations 7 | |
DOID:0090137 | complex cortical dysplasia with other brain malformations 1 | |
DOID:0110096 | short-rib thoracic dysplasia 14 with polydactyly | |
DOID:0110892 | inflammatory bowel disease 1 | |
DOID:0110942 | autosomal recessive osteopetrosis 1 | |
DOID:0110946 | autosomal recessive osteopetrosis 7 | |
DOID:0111045 | platelet-type bleeding disorder 9 | |
DOID:0111056 | platelet-type bleeding disorder 3 | |
DOID:0111057 | platelet-type bleeding disorder 11 | |
DOID:0111135 | congenital generalized lipodystrophy type 1 |
HPO ID | HPO Term |
---|---|
HP:0000973 | Cutis laxa |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001263 | Global developmental delay |
HP:0001270 | Motor delay |
HP:0001290 | Generalized hypotonia |
HP:0001302 | Pachygyria |
HP:0001305 | Dandy-Walker malformation |
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