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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:12960 | acrocephalosyndactylia | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:2349 | arteriosclerosis | HGNC:7160 | Homo sapiens (human) | 4323 | MMP14 |
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| DOID:0110838 | Usher syndrome type 2A | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0110414 | retinitis pigmentosa 3 | MGI:1344037 | Mus musculus (house mouse) | 19893 | Rpgr |
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| DOID:0111008 | X-linked cone-rod dystrophy 1 | MGI:1344037 | Mus musculus (house mouse) | 19893 | Rpgr |
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| DOID:1686 | glaucoma | RGD:2202 | Rattus norvegicus (Norway rat) | 24225 | Bdnf |
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| DOID:0060367 | Parkinson's disease 1 | MGI:1277151 | Mus musculus (house mouse) | 20617 | Snca |
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| DOID:2229 | factor XI deficiency | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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| DOID:2217 | Bernard-Soulier syndrome | MGI:1333744 | Mus musculus (house mouse) | 14723 | Gp1ba |
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| DOID:1612 | breast cancer | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:9279 | hyperhomocysteinemia | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:10652 | Alzheimer's disease | HGNC:7809 | Homo sapiens (human) | 4804 | NGFR |
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| DOID:0050548 | hereditary sensory neuropathy | MGI:97383 | Mus musculus (house mouse) | 18211 | Ntrk1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:2732 | Rothmund-Thomson syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:10016 | multiple endocrine neoplasia type 2B | MGI:97902 | Mus musculus (house mouse) | 19713 | Ret |
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| DOID:0050547 | familial medullary thyroid carcinoma | MGI:97902 | Mus musculus (house mouse) | 19713 | Ret |
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| DOID:0050771 | pheochromocytoma | MGI:97902 | Mus musculus (house mouse) | 19713 | Ret |
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| DOID:0050773 | paraganglioma | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0111862 | congenital bilateral absence of vas deferens | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:5844 | myocardial infarction | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:14330 | Parkinson's disease | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:0050855 | renal fibrosis | RGD:2493 | Rattus norvegicus (Norway rat) | 24310 | Ace |
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| DOID:0050787 | juvenile polyposis syndrome | MGI:894293 | Mus musculus (house mouse) | 17128 | Smad4 |
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| DOID:0110859 | polycystic kidney disease 2 | MGI:1099818 | Mus musculus (house mouse) | 18764 | Pkd2 |
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