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:0003560 | Muscular dystrophy |
HP:0003577 | Congenital onset |
HP:0003593 | Infantile onset |
HP:0003623 | Neonatal onset |
HP:0003691 | Scapular winging |
HP:0003701 | Proximal muscle weakness |
HP:0003707 | Calf muscle pseudohypertrophy |
HP:0003712 | Skeletal muscle hypertrophy |
HP:0003803 | Type 1 muscle fiber predominance |
HP:0004374 | Hemiplegia/hemiparesis |
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 |
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