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:0050214 | Lambert-Eaton myasthenic syndrome | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050700 | cardiomyopathy | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060260 | ptosis |
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 |
---|---|---|---|
100689938 | ORENI59621 | ||
115583970 | SPAAU41798 | ||
447346 | Xenbase:XB-GENE-922662 | ||
100037186 | Xenbase:XB-GENE-6255238 | ||
493267 | Xenbase:XB-GENE-922650 | ||
101934259 | CHRPI24410 | ||
109318261 | CROPO25358 | ||
113454477 | PSETE02832 | ||
103816951 | SERCA11185 | ||
100397938 | CALJA11912 |
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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