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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:655 | inherited metabolic disorder | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:0112159 | autosomal dominant nonsyndromic deafness 78 | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:25777 | Homo sapiens (human) | 64864 | RFX7 |
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| DOID:5016 | hepatocellular clear cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:1380 | endometrial cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:14330 | Parkinson's disease | HGNC:30343 | Homo sapiens (human) | 23317 | DNAJC13 |
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| DOID:0050534 | congenital stationary night blindness | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:684 | hepatocellular carcinoma | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:1380 | endometrial cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:1520 | colon carcinoma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0111641 | autosomal recessive nonsyndromic deafness 94 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:0111526 | Mullerian aplasia and hyperandrogenism | HGNC:12783 | Homo sapiens (human) | 54361 | WNT4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:7148 | rheumatoid arthritis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:783 | end stage renal disease | HGNC:6144 | Homo sapiens (human) | 8516 | ITGA8 |
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| DOID:0050741 | alcohol dependence | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0080329 | cold-induced sweating syndrome 1 | HGNC:2364 | Homo sapiens (human) | 9244 | CRLF1 |
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| DOID:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0080625 | severe congenital neutropenia 1 | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:9884 | muscular dystrophy | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:2987 | familial mediterranean fever | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:7188 | autoimmune thyroiditis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:12361 | Graves' disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:9975 | cocaine dependence | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:5035 | Homo sapiens (human) | 3183 | HNRNPC |
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