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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:10763 | hypertension | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:0060614 | ulnar-mammary syndrome | MGI:98495 | Mus musculus (house mouse) | 21386 | Tbx3 |
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| DOID:0060287 | cornea plana | MGI:1202398 | Mus musculus (house mouse) | 16545 | Kera |
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| DOID:9352 | type 2 diabetes mellitus | RGD:62058 | Rattus norvegicus (Norway rat) | 29473 | Aoc3 |
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| DOID:9970 | obesity | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:14179 | X-linked agammaglobulinemia | HGNC:1133 | Homo sapiens (human) | 695 | BTK |
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| DOID:10652 | Alzheimer's disease | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:0060768 | Smith-Magenis syndrome | HGNC:9834 | Homo sapiens (human) | 10743 | RAI1 |
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| DOID:9970 | obesity | HGNC:6932 | Homo sapiens (human) | 4160 | MC4R |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:5419 | schizophrenia | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:10652 | Alzheimer's disease | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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| DOID:4947 | cholangiocarcinoma | RGD:69051 | Rattus norvegicus (Norway rat) | 59086 | Tgfb1 |
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| DOID:0060903 | thrombosis | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | MGI:894698 | Mus musculus (house mouse) | 20391 | Sgca |
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| DOID:0110877 | holoprosencephaly 11 | MGI:1926387 | Mus musculus (house mouse) | 57810 | Cdon |
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| DOID:14686 | Axenfeld-Rieger syndrome | HGNC:3800 | Homo sapiens (human) | 2296 | FOXC1 |
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| DOID:0050989 | episodic ataxia type 1 | MGI:96654 | Mus musculus (house mouse) | 16485 | Kcna1 |
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| DOID:0050793 | short QT syndrome | MGI:1341722 | Mus musculus (house mouse) | 16511 | Kcnh2 |
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| DOID:10652 | Alzheimer's disease | RGD:70487 | Rattus norvegicus (Norway rat) | 84353 | Ctnnb1 |
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| DOID:11476 | osteoporosis | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1287 | cardiovascular system disease | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:9352 | type 2 diabetes mellitus | MGI:2153588 | Mus musculus (house mouse) | 140491 | Ppp1r3a |
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