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:0070138 | autosomal recessive cutis laxa type IIIB | |
DOID:0070140 | autosomal recessive cutis laxa type IIC | |
DOID:0070141 | autosomal recessive cutis laxa type II classic type | |
DOID:0070142 | autosomal dominant cutis laxa | |
DOID:0080001 | bone disease | |
DOID:0080332 | bicuspid aortic valve disease | |
DOID:0080333 | aortic valve disease 1 | |
DOID:0080334 | aortic valve disease 2 | |
DOID:0080564 | congenital disorder of glycosylation Il | |
DOID:0090130 | cortical dysplasia-focal epilepsy syndrome |
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 |
---|---|---|---|
103239340 | CHLSB02773 | ||
108540639 | RHIBE04548 | ||
104666329 | RHIRO00210 | ||
100598741 | NOMLE01352 | ||
114586165 | PODMU28734 | ||
107562586 | SINGR70167 | ||
107569397 | SINGR95359 | ||
107592366 | SINGR22166 | ||
107599966 | SINGR61475 | ||
106842224 | EQUAS14028 |
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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