Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080201 | Peters plus syndrome | MGI:2685903 | Mus musculus (house mouse) | 381694 | B3glct |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
|
||
| DOID:2986 | IgA glomerulonephritis | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
|
||
| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
|
||
| DOID:5212 | congenital disorder of glycosylation | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
|
||
| DOID:28 | endocrine system disease | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
|
||
| DOID:2377 | multiple sclerosis | HGNC:928 | Homo sapiens (human) | 9334 | B4GALT5 |
|
||
| DOID:2377 | multiple sclerosis | HGNC:929 | Homo sapiens (human) | 9331 | B4GALT6 |
|
||
| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
|
||
| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
|
||
| DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
|
||
| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
|
||
| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | MGI:1342057 | Mus musculus (house mouse) | 14421 | B4galnt1 |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
|
||
| DOID:0070256 | congenital disorder of glycosylation type IId | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
|
||
| DOID:5212 | congenital disorder of glycosylation | RGD:620900 | Rattus norvegicus (Norway rat) | 24390 | B4galt1 |
|
||
| DOID:2986 | IgA glomerulonephritis | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
|
||
| DOID:28 | endocrine system disease | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
|
||
| DOID:5212 | congenital disorder of glycosylation | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
|
||
| DOID:0070256 | congenital disorder of glycosylation type IId | RGD:620900 | Rattus norvegicus (Norway rat) | 24390 | B4galt1 |
|
||
| DOID:2377 | multiple sclerosis | MGI:1927169 | Mus musculus (house mouse) | 56336 | B4galt5 |
|
||
| DOID:2377 | multiple sclerosis | RGD:1310062 | Rattus norvegicus (Norway rat) | 362275 | B4galt5 |
|
||
| DOID:2377 | multiple sclerosis | RGD:71046 | Rattus norvegicus (Norway rat) | 65196 | B4galt6 |
|
||
| DOID:2377 | multiple sclerosis | MGI:1928380 | Mus musculus (house mouse) | 56386 | B4galt6 |
|
