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:0003327 | Axial muscle weakness |
HP:0003388 | Easy fatigability |
HP:0003391 | Gowers sign |
HP:0003394 | Muscle spasm |
HP:0003403 | EMG: decremental response of compound muscle action potential to repetitive nerve stimulation |
HP:0003457 | EMG abnormality |
HP:0003473 | Fatigable weakness |
HP:0003546 | Exercise intolerance |
HP:0003549 | Abnormality of connective tissue |
HP:0003551 | Difficulty climbing stairs |
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 |
---|---|---|---|
112911432 | VULVU03917 | ||
123798672 | URSAM07433 | ||
101673791 | MUSPF09815 | ||
101086635 | FELCA04827 | ||
122214353 | PANLE23196 | ||
101318382 | TURTR07378 | ||
514161 | BOVIN17824 | ||
102178496 | CAPHI14717 | ||
101102764 | SHEEP08442 | ||
105994575 | DIPOR18777 |
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