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:0060261 | congenital ptosis | |
DOID:0060305 | megalocornea | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
DOID:0080092 | myofibrillar myopathy 1 | |
DOID:0080094 | myofibrillar myopathy 3 | |
DOID:0110213 | isolated cleft palate | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A |
HPO ID | HPO Term |
---|---|
HP:0000568 | Microphthalmia |
HP:0000580 | Pigmentary retinopathy |
HP:0000589 | Coloboma |
HP:0000609 | Optic nerve hypoplasia |
HP:0000618 | Blindness |
HP:0000639 | Nystagmus |
HP:0000648 | Optic atrophy |
HP:0000707 | Abnormality of the nervous system |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
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 |
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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