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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:1388 | Tangier disease | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:3210 | Pelizaeus-Merzbacher disease | HGNC:9086 | Homo sapiens (human) | 5354 | PLP1 |
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| DOID:13141 | uveitis | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0050741 | alcohol dependence | HGNC:4070 | Homo sapiens (human) | 2550 | GABBR1 |
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| DOID:8354 | complement component 3 deficiency | MGI:88227 | Mus musculus (house mouse) | 12266 | C3 |
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| DOID:0111011 | cone-rod dystrophy 6 | MGI:105123 | Mus musculus (house mouse) | 14919 | Gucy2e |
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| DOID:3883 | Lynch syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | MGI:104903 | Mus musculus (house mouse) | 14734 | Gpc3 |
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| DOID:3413 | alpha-mannosidosis | MGI:107286 | Mus musculus (house mouse) | 17159 | Man2b1 |
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| DOID:418 | systemic scleroderma | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9291 | Homo sapiens (human) | 5506 | PPP1R3A |
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| DOID:0111046 | platelet-type bleeding disorder 10 | MGI:107899 | Mus musculus (house mouse) | 12491 | Cd36 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:0111029 | hemochromatosis type 1 | MGI:109191 | Mus musculus (house mouse) | 15216 | Hfe |
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| DOID:0110007 | achromatopsia 2 | MGI:1341818 | Mus musculus (house mouse) | 12790 | Cnga3 |
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| DOID:4480 | achondroplasia | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0060745 | Doyne honeycomb retinal dystrophy | HGNC:3218 | Homo sapiens (human) | 2202 | EFEMP1 |
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| DOID:2729 | dyskeratosis congenita | HGNC:2890 | Homo sapiens (human) | 1736 | DKC1 |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | MGI:95392 | Mus musculus (house mouse) | 13805 | Eng |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3544 | Homo sapiens (human) | 2155 | F7 |
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| DOID:3068 | glioblastoma | RGD:620349 | Rattus norvegicus (Norway rat) | 29527 | Ptgs2 |
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| DOID:11211 | buphthalmos | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:7148 | rheumatoid arthritis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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