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:0003560 | Muscular dystrophy |
HP:0003577 | Congenital onset |
HP:0003593 | Infantile onset |
HP:0003623 | Neonatal onset |
HP:0003691 | Scapular winging |
HP:0003701 | Proximal muscle weakness |
HP:0003707 | Calf muscle pseudohypertrophy |
HP:0003712 | Skeletal muscle hypertrophy |
HP:0003803 | Type 1 muscle fiber predominance |
HP:0004374 | Hemiplegia/hemiparesis |
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 |
---|---|---|---|
103227639 | CHLSB10361 | ||
108526985 | RHIBE18890 | ||
104667304 | RHIRO13974 | ||
100583111 | NOMLE29513 | ||
114591493 | PODMU13848 | ||
107588415 | SINGR42925 | ||
116816499 | CHEAB22838 | ||
105311242 | PTEVA16189 | ||
115043662 | ECHNA04773 | ||
115388098 | SALFA35913 |
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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