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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:684 | hepatocellular carcinoma | MGI:108360 | Mus musculus (house mouse) | 13800 | Enah |
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| DOID:0081150 | common variable immunodeficiency 7 | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:9261 | nasopharynx carcinoma | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:14648 | Homo sapiens (human) | 137994 | LETM2 |
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| DOID:0050460 | Wolf-Hirschhorn syndrome | HGNC:14648 | Homo sapiens (human) | 137994 | LETM2 |
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| DOID:9884 | muscular dystrophy | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:0050700 | cardiomyopathy | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:0110436 | dilated cardiomyopathy 1L | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:12365 | malaria | HGNC:2334 | Homo sapiens (human) | 1378 | CR1 |
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| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0110805 | hereditary spastic paraplegia 53 | HGNC:24928 | Homo sapiens (human) | 137492 | VPS37A |
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| DOID:9970 | obesity | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:12351 | alcoholic hepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:783 | end stage renal disease | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:1094 | attention deficit hyperactivity disorder | MGI:106912 | Mus musculus (house mouse) | 13733 | Adgre1 |
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| DOID:3891 | placental insufficiency | MGI:1098726 | Mus musculus (house mouse) | 13731 | Emp2 |
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