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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:1184 | nephrotic syndrome | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:3459 | breast carcinoma | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:0050827 | rheumatic heart disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0050591 | tooth agenesis | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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| DOID:1682 | congenital heart disease | HGNC:3122 | Homo sapiens (human) | 7044 | LEFTY2 |
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| DOID:9538 | multiple myeloma | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:5844 | myocardial infarction | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:655 | inherited metabolic disorder | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:418 | systemic scleroderma | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0050580 | hereditary lymphedema | HGNC:17754 | Homo sapiens (human) | 55901 | THSD1 |
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| DOID:5082 | liver cirrhosis | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:1686 | glaucoma | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10652 | Alzheimer's disease | HGNC:9206 | Homo sapiens (human) | 5446 | PON3 |
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| DOID:1324 | lung cancer | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:0112242 | congenital symmetric circumferential skin creases 1 | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
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| DOID:2320 | obstructive lung disease | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:0111302 | generalized epilepsy with febrile seizures plus 1 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:12377 | spinal muscular atrophy | HGNC:3010 | Homo sapiens (human) | 1804 | DPP6 |
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| DOID:0111806 | syndromic microphthalmia 5 | HGNC:8522 | Homo sapiens (human) | 5015 | OTX2 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17348 | Homo sapiens (human) | 9129 | PRPF3 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0050654 | Baller-Gerold syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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