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 |
---|---|---|
Golgi membrane |
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:0060771 | obsolete dextro-looped transposition of the great arteries 1 | |
DOID:0060772 | multiple types of congenital heart defects 6 | |
DOID:0060807 | syndromic X-linked intellectual disability Najm type | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0060857 | septooptic dysplasia | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
DOID:0080033 | craniometaphyseal dysplasia | |
DOID:0080092 | myofibrillar myopathy 1 | |
DOID:0080094 | myofibrillar myopathy 3 | |
DOID:0080102 | congenital myopathy 4A |
HPO ID | HPO Term |
---|---|
HP:0000648 | Optic atrophy |
HP:0000659 | Peters anomaly |
HP:0000750 | Delayed speech and language development |
HP:0000767 | Pectus excavatum |
HP:0000969 | Edema |
HP:0001105 | Retinal atrophy |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001262 | Excessive daytime somnolence |
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 |
---|---|---|---|
173469 | WB:WBGene00020307 | ||
188207 | WB:WBGene00011554 | ||
189104 | WB:WBGene00020924 | ||
189107 | WB:WBGene00020927 | ||
189504 | WB:WBGene00021249 | ||
100006345 | ZFIN:ZDB-GENE-070410-96 | DANRE35456 | |
108259698 | ICTPU23339 | ||
113582820 | ELEEL30070 | ||
115160178 | SALTR70125 | ||
115531894 | GADMO24802 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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