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:0002540 | Inability to walk |
HP:0002650 | Scoliosis |
HP:0002827 | Hip dislocation |
HP:0002828 | Multiple joint contractures |
HP:0002878 | Respiratory failure |
HP:0002938 | Lumbar hyperlordosis |
HP:0003198 | Myopathy |
HP:0003200 | Ragged-red muscle fibers |
HP:0003236 | Elevated circulating creatine kinase concentration |
HP:0003325 | Limb-girdle muscle weakness |
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