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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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Repository for lectin-assisted multimodality data
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MIRAGE
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:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:9008 | psoriatic arthritis | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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| DOID:13241 | Behcet's disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:1702 | ichthyosis vulgaris | HGNC:3748 | Homo sapiens (human) | 2312 | FLG |
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| DOID:3526 | cerebral infarction | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0081137 | agammaglobulinemia 3 | HGNC:1698 | Homo sapiens (human) | 973 | CD79A |
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| DOID:1287 | cardiovascular system disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:0111498 | combined oxidative phosphorylation deficiency 22 | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:3652 | Leigh disease | HGNC:7461 | Homo sapiens (human) | 4540 | MT-ND5 |
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| DOID:0080238 | autosomal dominant intellectual developmental disorder 47 | HGNC:11354 | Homo sapiens (human) | 10274 | STAG1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2859 | Homo sapiens (human) | 1718 | DHCR24 |
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| DOID:10283 | prostate cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3119 | gastrointestinal system cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:0060584 | Noonan syndrome 6 | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:11123 | Henoch-Schoenlein purpura | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:2349 | arteriosclerosis | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:1324 | lung cancer | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:0050578 | occult macular dystrophy | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:23150 | Homo sapiens (human) | 23025 | UNC13A |
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| DOID:612 | primary immunodeficiency disease | HGNC:10937 | Homo sapiens (human) | 6573 | SLC19A1 |
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| DOID:0110704 | hypotrichosis 7 | HGNC:18483 | Homo sapiens (human) | 200879 | LIPH |
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| DOID:8692 | myeloid leukemia | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0110698 | hypotrichosis 1 | HGNC:15718 | Homo sapiens (human) | 147495 | APCDD1 |
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| DOID:12241 | beta thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1389 | polyneuropathy | HGNC:11181 | Homo sapiens (human) | 6649 | SOD3 |
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