UniProt | Protein Name |
---|---|
O95528 |
|
GO Term | Evidence Code | PMID |
---|---|---|
dehydroascorbic acid transport | ||
glucose transmembrane transport | ||
galactose transmembrane transport |
|
|
embryonic skeletal joint development | ||
cell redox homeostasis |
GO Term | Evidence Code | PMID |
---|---|---|
carbohydrate:proton symporter activity |
|
|
symporter activity | ||
D-glucose transmembrane transporter activity | ||
dehydroascorbic acid transmembrane transporter activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050429 | Hailey-Hailey disease | |
DOID:0050466 | Loeys-Dietz syndrome | |
DOID:0050645 | arterial tortuosity syndrome | |
DOID:0050700 | cardiomyopathy | |
DOID:0050830 | peripheral artery disease | |
DOID:0060249 | scoliosis | |
DOID:0060305 | megalocornea | |
DOID:0060319 | cardiac arrest | |
DOID:0060320 | inguinal hernia |
HPO ID | HPO Term |
---|---|
HP:0001582 | Redundant skin |
HP:0001635 | Congestive heart failure |
HP:0001637 | Abnormal myocardium morphology |
HP:0001639 | Hypertrophic cardiomyopathy |
HP:0001644 | Dilated cardiomyopathy |
HP:0001650 | Aortic valve stenosis |
HP:0001658 | Myocardial infarction |
HP:0001659 | Aortic regurgitation |
HP:0001695 | Cardiac arrest |
HP:0001714 | Ventricular hypertrophy |
Disease ID | Disease Name |
---|---|
OMIM:208050 |
|
ORPHA:3342 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
366251 | RGD:1306552 | RATNO26472 | |
100731003 | CAVPO16545 | ||
101582471 | OCTDE14086 | ||
101873451 | MELUD11811 | ||
100029696 | MONDO03248 | ||
102447112 | PELSI12135 | ||
103669697 | URSMA14531 | ||
114033299 | VOMUR11146 | ||
113902941 | BOBOX02973 | ||
100943755 | OTOGA13803 |
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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