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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:0070425 | combined oxidative phosphorylation deficiency 52 | HGNC:15910 | Homo sapiens (human) | 9054 | NFS1 |
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| DOID:4448 | macular degeneration | HGNC:7166 | Homo sapiens (human) | 4313 | MMP2 |
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| DOID:14415 | Legg-Calve-Perthes disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1799 | islet cell tumor | HGNC:2681 | Homo sapiens (human) | 1616 | DAXX |
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| DOID:783 | end stage renal disease | HGNC:338 | Homo sapiens (human) | 186 | AGTR2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0081164 | dilated cardiomyopathy 3B | HGNC:2928 | Homo sapiens (human) | 1756 | DMD |
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| DOID:0080090 | reducing body myopathy 1A | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:12361 | Graves' disease | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:0110542 | autosomal dominant nonsyndromic deafness 10 | HGNC:3522 | Homo sapiens (human) | 2070 | EYA4 |
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| DOID:2377 | multiple sclerosis | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:9352 | type 2 diabetes mellitus | RGD:1308135 | Rattus norvegicus (Norway rat) | 361722 | Bscl2 |
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| DOID:9538 | multiple myeloma | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:9970 | obesity | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:1596 | depressive disorder | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:0060241 | 3-M syndrome | HGNC:29092 | Homo sapiens (human) | 23363 | OBSL1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:0050984 | spinocerebellar ataxia type 37 | HGNC:2661 | Homo sapiens (human) | 1600 | DAB1 |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:9958 | Homo sapiens (human) | 5972 | REN |
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| DOID:0111941 | immunodeficiency 20 | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0070013 | Seckel syndrome 2 | HGNC:9891 | Homo sapiens (human) | 5932 | RBBP8 |
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| DOID:12377 | spinal muscular atrophy | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:11712 | lipoatrophic diabetes mellitus | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0111010 | cone-rod dystrophy 5 | HGNC:21043 | Homo sapiens (human) | 83394 | PITPNM3 |
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