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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0080726 | Ehlers-Danlos syndrome classic type 2 | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:14720 | Ehlers-Danlos syndrome classic type 1 | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:850 | lung disease | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:0081386 | TANGO2-related metabolic encephalopathy and arrythmias | HGNC:25439 | Homo sapiens (human) | 128989 | TANGO2 |
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| DOID:936 | brain disease | MGI:109176 | Mus musculus (house mouse) | 12896 | Cpt2 |
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| DOID:0080000 | muscular disease | MGI:109176 | Mus musculus (house mouse) | 12896 | Cpt2 |
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| DOID:3146 | lipid metabolism disorder | MGI:109176 | Mus musculus (house mouse) | 12896 | Cpt2 |
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| DOID:3319 | lymphangioleiomyomatosis | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:9970 | obesity | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:3146 | lipid metabolism disorder | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:12351 | alcoholic hepatitis | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:783 | end stage renal disease | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:409 | liver disease | MGI:104841 | Mus musculus (house mouse) | 12892 | Cpox |
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| DOID:13269 | hereditary coproporphyria | MGI:104841 | Mus musculus (house mouse) | 12892 | Cpox |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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| DOID:14720 | Ehlers-Danlos syndrome classic type 1 | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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