GO Term | Evidence Code | PMID |
---|---|---|
protein O-linked glycosylation | ||
nervous system development |
|
|
muscle organ development |
|
|
negative regulation of cell population proliferation | ||
regulation of protein glycosylation |
|
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
endoplasmic reticulum | ||
cis-Golgi network | ||
extracellular space |
|
|
Golgi apparatus |
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | XP_342839 | XM_342838 |
Caenorhabditis elegans | NP_497236 | NM_064835 |
Mus musculus | NP_647470 | NM_139309 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | |
DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | |
DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N |
HPO ID | HPO Term |
---|---|
HP:0001305 | Dandy-Walker malformation |
HP:0001319 | Neonatal hypotonia |
HP:0001321 | Cerebellar hypoplasia |
HP:0001324 | Muscle weakness |
HP:0001328 | Specific learning disability |
HP:0001331 | Absent septum pellucidum |
HP:0001339 | Lissencephaly |
HP:0001344 | Absent speech |
HP:0001349 | Facial diplegia |
HP:0001357 | Plagiocephaly |
Disease ID | Disease Name |
---|---|
ORPHA:370980 |
|
ORPHA:154 |
|
ORPHA:899 |
|
OMIM:613152 |
|
ORPHA:272 |
|
OMIM:236670 |
|
OMIM:253800 |
|
OMIM:611588 |
|
ORPHA:588 |
|
OMIM:611615 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115619890 | STRHB08052 |
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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