UniProt | Protein Name |
---|---|
A0A140VJM1 |
|
A4D126 |
|
GO Term | Evidence Code | PMID |
---|---|---|
isoprenoid biosynthetic process | ||
axon guidance | ||
protein O-linked mannosylation |
GO Term | Evidence Code | PMID |
---|---|---|
D-ribitol-5-phosphate cytidylyltransferase activity | ||
protein homodimerization activity | ||
cytidylyltransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:11719 | oculopharyngeal muscular dystrophy | |
DOID:11720 | distal myopathy | |
DOID:11723 | Duchenne muscular dystrophy | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:11727 | facioscapulohumeral muscular dystrophy | |
DOID:11832 | visual epilepsy | |
DOID:12270 | coloboma | |
DOID:14159 | obstructive hydrocephalus | |
DOID:14524 | senile degeneration of brain | |
DOID:14686 | Axenfeld-Rieger syndrome |
HPO ID | HPO Term |
---|---|
HP:0001284 | Areflexia |
HP:0001288 | Gait disturbance |
HP:0001290 | Generalized hypotonia |
HP:0001302 | Pachygyria |
HP:0001305 | Dandy-Walker malformation |
HP:0001319 | Neonatal hypotonia |
HP:0001321 | Cerebellar hypoplasia |
HP:0001324 | Muscle weakness |
HP:0001328 | Specific learning disability |
HP:0001331 | Absent septum pellucidum |
Disease ID | Disease Name |
---|---|
ORPHA:370980 |
|
ORPHA:352479 |
|
OMIM:616052 |
|
ORPHA:899 |
|
OMIM:614643 |
|
ORPHA:588 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
104968457 | BOVIN27712 | ||
102187829 | CAPHI23970 | ||
100337768 | RABIT14426 | ||
75847 | MGI:1923097 | MOUSE08853 | |
493574 | RGD:1359368 | RATNO35992 | |
100946143 | OTOGA17955 | ||
105716156 | AOTNA04192 | ||
101028455 | SAIBB30447 | ||
101974291 | ICTTR09821 | ||
102417983 | MYOLU02671 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024