UniProt | Protein Name |
---|---|
Q9Y5P6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein glycosylation | ||
GDP-mannose biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
mannose-1-phosphate guanylyltransferase (GTP) activity | ||
GTP binding | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:11723 | Duchenne muscular dystrophy | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:11727 | facioscapulohumeral muscular dystrophy | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:11830 | myopia | |
DOID:11832 | visual epilepsy | |
DOID:11836 | clubfoot | |
DOID:11984 | hypertrophic cardiomyopathy | |
DOID:12215 | oligohydramnios | |
DOID:12270 | coloboma |
HPO ID | HPO Term |
---|---|
HP:0004637 | Decreased cervical spine mobility |
HP:0006380 | Knee flexion contracture |
HP:0006698 | Dilatation of the ventricular cavity |
HP:0006899 | Fusion of the cerebellar hemispheres |
HP:0006955 | Olivopontocerebellar hypoplasia |
HP:0007015 | Poor gross motor coordination |
HP:0007204 | Diffuse white matter abnormalities |
HP:0007256 | Abnormal pyramidal sign |
HP:0007260 | Type II lissencephaly |
HP:0007340 | Lower limb muscle weakness |
Disease ID | Disease Name |
---|---|
ORPHA:363623 |
|
ORPHA:370968 |
|
ORPHA:370959 |
|
OMIM:615351 |
|
OMIM:615350 |
|
ORPHA:353327 |
|
ORPHA:588 |
|
OMIM:615352 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105823928 | PROCO00286 | ||
851504 | SGD:S000002213 | ||
109060948 | CYPCA144445 | ||
109065924 | CYPCA144445 | ||
103750182 | NANGA14017 | ||
116449609 | CORMO01659 | ||
103265510 | CARSF09751 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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