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:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050453 | lissencephaly | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050777 | Joubert syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060270 | pontocerebellar hypoplasia type 2D |
HPO ID | HPO Term |
---|---|
HP:0000358 | Posteriorly rotated ears |
HP:0000369 | Low-set ears |
HP:0000411 | Protruding ear |
HP:0000478 | Abnormality of the eye |
HP:0000482 | Microcornea |
HP:0000486 | Strabismus |
HP:0000490 | Deeply set eye |
HP:0000501 | Glaucoma |
HP:0000505 | Visual impairment |
HP:0000518 | Cataract |
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 |
---|---|---|---|
744905 | PANTR39748 | ||
100436260 | PONAB33726 | ||
100477709 | AILME14636 | ||
101685841 | MUSPF17497 | ||
101092257 | FELCA03452 | ||
122208353 | PANLE23267 | ||
101316792 | TURTR14626 | ||
118900802 | BALMU12488 | ||
100658658 | LOXAF17662 | ||
100065851 | HORSE33072 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024