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:0050214 | Lambert-Eaton myasthenic syndrome | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050700 | cardiomyopathy | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060260 | ptosis |
HPO ID | HPO Term |
---|---|
HP:0009055 | Generalized limb muscle atrophy |
HP:0010628 | Facial palsy |
HP:0010864 | Intellectual disability, severe |
HP:0011102 | Ileal atresia |
HP:0011463 | Childhood onset |
HP:0011968 | Feeding difficulties |
HP:0012110 | Hypoplasia of the pons |
HP:0012443 | Abnormal brain morphology |
HP:0012695 | Decreased thalamic volume |
HP:0100022 | Abnormality of movement |
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 |
---|---|---|---|
100760573 | CRIGR07385 | ||
331026 | MGI:2660880 | MOUSE61930 | |
363145 | RGD:1560458 | ||
100735495 | CAVPO04827 | ||
101578564 | OCTDE02644 | ||
101716745 | HETGA06531 | ||
100028039 | MONDO30686 | ||
100566017 | ANOCA03420 | ||
114024188 | VOMUR13929 | ||
100957489 | OTOGA02941 |
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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