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:0110881 | holoprosencephaly 1 | |
DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | |
DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | |
DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
DOID:0111531 | bilateral optic nerve hypoplasia | |
DOID:0112374 | muscular dystrophy-dystroglycanopathy | |
DOID:1029 | familial periodic paralysis | |
DOID:10293 | monocular esotropia | |
DOID:10375 | strabismic amblyopia | |
DOID:10376 | amblyopia |
HPO ID | HPO Term |
---|---|
HP:0000478 | Abnormality of the eye |
HP:0000485 | Megalocornea |
HP:0000486 | Strabismus |
HP:0000501 | Glaucoma |
HP:0000505 | Visual impairment |
HP:0000508 | Ptosis |
HP:0000518 | Cataract |
HP:0000525 | Abnormality iris morphology |
HP:0000541 | Retinal detachment |
HP:0000545 | Myopia |
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 |
---|---|---|---|
183400 | WB:WBGene00016583 | ||
40599 | FB:FBgn0037279 | ||
103176754 | CALMI10811 | ||
102359278 | LATCH03221 | ||
445097 | ZFIN:ZDB-GENE-040801-234 | DANRE22403 | |
103040139 | ASTMX00781 | ||
108255040 | ICTPU16618 | ||
113572399 | ELEEL11483 | ||
115149997 | SALTR34613 | ||
101163000 | ORYLA14536 |
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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