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:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000028 | Cryptorchidism |
HP:0000160 | Narrow mouth |
HP:0000218 | High palate |
HP:0000252 | Microcephaly |
HP:0000253 | Progressive microcephaly |
HP:0000260 | Wide anterior fontanel |
HP:0000270 | Delayed cranial suture closure |
HP:0000272 | Malar flattening |
Disease ID | Disease Name |
---|---|
OMIM:219200 |
|
ORPHA:357074 |
|
OMIM:278250 |
|
ORPHA:2834 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100766909 | CRIGR17212 | ||
21871 | MGI:104855 | MOUSE44675 | |
116455 | RGD:621006 | ||
101787762 | CAVPO22728 | ||
101569632 | OCTDE15102 | ||
103101820 | MONDO18514 | ||
102449285 | PELSI03939 | ||
102449675 | PELSI03939 | ||
103661250 | URSMA18001 | ||
101071950 | TAKRU43980 |
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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