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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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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:0110647 | long QT syndrome 5 | HGNC:6240 | Homo sapiens (human) | 3753 | KCNE1 |
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| DOID:11724 | limb-girdle muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:3490 | Noonan syndrome | HGNC:11187 | Homo sapiens (human) | 6654 | SOS1 |
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| DOID:0060673 | Peters anomaly | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:1389 | polyneuropathy | HGNC:11181 | Homo sapiens (human) | 6649 | SOD3 |
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| DOID:0070454 | hereditary spastic paraplegia 70 | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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| DOID:10283 | prostate cancer | HGNC:6190 | Homo sapiens (human) | 3716 | JAK1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:609 | Homo sapiens (human) | 344 | APOC2 |
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| DOID:0060304 | dyschromatosis universalis hereditaria | HGNC:47 | Homo sapiens (human) | 10058 | ABCB6 |
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| DOID:3454 | brain infarction | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:2377 | multiple sclerosis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:1324 | lung cancer | HGNC:1960 | Homo sapiens (human) | 1139 | CHRNA7 |
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| DOID:3385 | bacterial vaginosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:11476 | osteoporosis | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:2841 | asthma | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:848 | arthritis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:8454 | riboflavin deficiency | HGNC:30225 | Homo sapiens (human) | 55065 | SLC52A1 |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:3312 | bipolar disorder | HGNC:5295 | Homo sapiens (human) | 3358 | HTR2C |
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| DOID:1062 | Fanconi syndrome | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:4253 | melorheostosis | HGNC:6840 | Homo sapiens (human) | 5604 | MAP2K1 |
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| DOID:0080681 | X-linked chronic idiopathic intestinal pseudo-obstruction | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:12987 | agranulocytosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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