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:1756 | facial nerve disease | |
DOID:1826 | epilepsy | |
DOID:1827 | idiopathic generalized epilepsy | |
DOID:3635 | congenital myasthenic syndrome | |
DOID:4090 | agnosia | |
DOID:422 | congenital structural myopathy | |
DOID:423 | myopathy | |
DOID:4621 | holoprosencephaly | |
DOID:5327 | retinal detachment | |
DOID:539 | ophthalmoplegia |
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 |
---|---|---|---|
101080238 | TAKRU20069 | ||
102015564 | CHILA22607 | ||
105727702 | AOTNA35725 | ||
110217035 | PHACI11820 | ||
101047504 | SAIBB27149 | ||
101969114 | ICTTR14799 | ||
101596642 | JACJA15670 | ||
118308814 | SCOMX26827 | ||
117036807 | RHIFE15945 | ||
101816657 | FICAL12803 |
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