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:0002540 | Inability to walk |
HP:0002650 | Scoliosis |
HP:0002827 | Hip dislocation |
HP:0002828 | Multiple joint contractures |
HP:0002878 | Respiratory failure |
HP:0002938 | Lumbar hyperlordosis |
HP:0003198 | Myopathy |
HP:0003200 | Ragged-red muscle fibers |
HP:0003236 | Elevated circulating creatine kinase concentration |
HP:0003325 | Limb-girdle 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 |
---|---|---|---|
105573696 | CERAT32380 | ||
705454 | MACMU29533 | ||
105480447 | MACNE07039 | ||
101018643 | PAPAN24657 | ||
105540343 | MANLE07261 | ||
101142350 | GORGO29480 | ||
100986111 | PANPA27885 | ||
460378 | PANTR31162 | ||
100436355 | PONAB25882 | ||
100856660 | CANLF07498 |
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