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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▲ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1312 | focal segmental glomerulosclerosis | HGNC:18290 | Homo sapiens (human) | 55907 | CMAS |
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| DOID:0110219 | Brugada syndrome 2 | HGNC:28956 | Homo sapiens (human) | 23171 | GPD1L |
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| DOID:0050647 | Arts syndrome | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:2377 | multiple sclerosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9970 | obesity | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:423 | myopathy | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:9452 | steatotic liver disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:10652 | Alzheimer's disease | HGNC:389 | Homo sapiens (human) | 8574 | AKR7A2 |
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| DOID:3070 | high grade glioma | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:13603 | obstructive jaundice | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:13001 | carotid stenosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:9975 | cocaine dependence | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:1612 | breast cancer | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:0050073 | invasive aspergillosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:10283 | prostate cancer | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:2987 | familial mediterranean fever | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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