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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:303 | substance-related disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:1287 | cardiovascular system disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050127 | sinusitis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:0070113 | Niemann-Pick disease type C1 | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
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| DOID:5419 | schizophrenia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:10652 | Alzheimer's disease | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:0111162 | epidermal nevus | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:13375 | temporal arteritis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4398 | pustulosis of palm and sole | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:14330 | Parkinson's disease | HGNC:256 | Homo sapiens (human) | 131 | ADH7 |
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| DOID:13378 | Kawasaki disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:5041 | esophageal cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:1574 | alcohol use disorder | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:13544 | low tension glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:3892 | insulinoma | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0050741 | alcohol dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:12678 | hypercalcemia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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