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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:0050426 | Stevens-Johnson syndrome | MGI:95935 | Mus musculus (house mouse) | 110557 | H2-Q6 |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95959 | Mus musculus (house mouse) | 15043 | H2-T3 |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95936 | Mus musculus (house mouse) | 15018 | H2-Q7 |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95931 | Mus musculus (house mouse) | 15013 | H2-Q2 |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95914 | Mus musculus (house mouse) | 14990 | H2-M2 |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95929 | Mus musculus (house mouse) | 15007 | H2-Q10 |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95933 | Mus musculus (house mouse) | 15015 | H2-Q4 |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050426 | Stevens-Johnson syndrome | MGI:95928 | Mus musculus (house mouse) | 15006 | H2-Q1 |
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| DOID:0050817 | Stargardt disease | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
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| DOID:0050817 | Stargardt disease | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050817 | Stargardt disease | MGI:1933331 | Mus musculus (house mouse) | 83603 | Elovl4 |
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| DOID:0050817 | Stargardt disease | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0112104 | Sotos syndrome 3 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0112102 | Sotos syndrome 2 | HGNC:7788 | Homo sapiens (human) | 4784 | NFIX |
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| DOID:0112102 | Sotos syndrome 2 | MGI:97311 | Mus musculus (house mouse) | 18032 | Nfix |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:12767 | Homo sapiens (human) | 54904 | NSD3 |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:12766 | Homo sapiens (human) | 7468 | NSD2 |
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| DOID:14748 | Sotos syndrome | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:0090114 | Sorsby's fundus dystrophy | WB:WBGene00019478 | Caenorhabditis elegans | 179197 | cri-2 |
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| DOID:0090114 | Sorsby's fundus dystrophy | MGI:98754 | Mus musculus (house mouse) | 21859 | Timp3 |
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| DOID:0090114 | Sorsby's fundus dystrophy | HGNC:11822 | Homo sapiens (human) | 7078 | TIMP3 |
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