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 |
---|---|---|
focal adhesion | ||
phagocytic vesicle membrane |
|
|
lysosomal membrane | ||
perinuclear region of cytoplasm | ||
vacuolar proton-transporting V-type ATPase complex |
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:0008947 | Infantile muscular hypotonia |
HP:0009004 | Hypoplasia of the musculature |
HP:0009125 | Lipodystrophy |
HP:0010719 | Abnormality of hair texture |
HP:0010838 | High nonceruloplasmin-bound serum copper |
HP:0010989 | Abnormality of the intrinsic pathway |
HP:0011003 | High myopia |
HP:0011623 | Muscular ventricular septal defect |
HP:0011800 | Midface retrusion |
HP:0011968 | Feeding difficulties |
Disease ID | Disease Name |
---|---|
OMIM:219200 |
|
ORPHA:357074 |
|
OMIM:278250 |
|
ORPHA:2834 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174743 | WB:WBGene00006915 | ||
176257 | WB:WBGene00006768 | ||
177626 | WB:WBGene00006914 | ||
178219 | WB:WBGene00006916 | ||
34587 | FB:FBgn0032373 | ||
42214 | FB:FBgn0038613 | ||
246543 | FB:FBgn0028669 | ||
103188002 | CALMI38026 | ||
102351124 | LATCH18385 | ||
561117 | ZFIN:ZDB-GENE-060526-4 | DANRE36906 |
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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