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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:14115 | toxic shock syndrome | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080582 | hypotrichosis 14 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:162 | cancer | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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| DOID:0060326 | myelomeningocele | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:1324 | lung cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3526 | cerebral infarction | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:10754 | otitis media | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:5016 | hepatocellular clear cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0060322 | mastoiditis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:2615 | papilloma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:5844 | myocardial infarction | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:8778 | Crohn's disease | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0050770 | polycystic liver disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:10584 | retinitis pigmentosa | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:83 | cataract | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:0080626 | corticosterone methyloxidase deficiency 1 | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:0060224 | atrial fibrillation | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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