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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:13241 | Behcet's disease | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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| DOID:783 | end stage renal disease | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:0080787 | proximal symphalangism 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:0110402 | retinitis pigmentosa 45 | HGNC:2151 | Homo sapiens (human) | 1258 | CNGB1 |
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| DOID:11832 | visual epilepsy | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:3121 | gallbladder cancer | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:0111631 | familial erythrocytosis 7 | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:3312 | bipolar disorder | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:216 | dental caries | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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| DOID:0111359 | large congenital melanocytic nevus | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:0060181 | ischemic colitis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:3310 | atopic dermatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0060903 | thrombosis | HGNC:5181 | Homo sapiens (human) | 3273 | HRG |
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| DOID:0080931 | primary localized cutaneous amyloidosis 2 | HGNC:18969 | Homo sapiens (human) | 133396 | IL31RA |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:3507 | dermatofibrosarcoma protuberans | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12678 | hypercalcemia | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:2841 | asthma | HGNC:4947 | Homo sapiens (human) | 3122 | HLA-DRA |
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| DOID:11695 | portal vein thrombosis | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
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| DOID:0111999 | immunodeficiency 61 | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:25240 | Homo sapiens (human) | 196527 | ANO6 |
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| DOID:0110187 | Charcot-Marie-Tooth disease type 4K | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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