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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:2217 | Bernard-Soulier syndrome | HGNC:4444 | Homo sapiens (human) | 2815 | GP9 |
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| DOID:8577 | ulcerative colitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2738 | pseudoxanthoma elasticum | RGD:620268 | Rattus norvegicus (Norway rat) | 81642 | Abcc6 |
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| DOID:684 | hepatocellular carcinoma | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:88385 | Mus musculus (house mouse) | 12628 | Cfh |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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| DOID:0110933 | nemaline myopathy 11 | MGI:1916052 | Mus musculus (house mouse) | 68802 | Mypn |
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| DOID:0080433 | developmental and epileptic encephalopathy 51 | SGD:S000001568 | Saccharomyces cerevisiae S288C | 853777 | MDH1 |
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| DOID:1742 | drug psychosis | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0060041 | autism spectrum disorder | MGI:1298205 | Mus musculus (house mouse) | 20539 | Slc7a5 |
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| DOID:10487 | Hirschsprung's disease | ZFIN:ZDB-GENE-980526-307 | Danio rerio (zebrafish) | 30512 | ret |
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| DOID:0080642 | Middle East respiratory syndrome | MGI:94919 | Mus musculus (house mouse) | 13482 | Dpp4 |
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| DOID:0080181 | PHARC syndrome | ZFIN:ZDB-GENE-060929-268 | Danio rerio (zebrafish) | 767657 | abhd12 |
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| DOID:0080350 | retinitis pigmentosa 77 | MGI:1917585 | Mus musculus (house mouse) | 70335 | Reep6 |
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| DOID:8670 | eating disorder | MGI:3036234 | Mus musculus (house mouse) | 208727 | Hdac4 |
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| DOID:9976 | heroin dependence | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:10762 | portal hypertension | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:3209 | junctional epidermolysis bullosa | MGI:99909 | Mus musculus (house mouse) | 16774 | Lama3 |
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| DOID:0070151 | hereditary sensory and autonomic neuropathy type 6 | MGI:104627 | Mus musculus (house mouse) | 13518 | Dst |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | MGI:96692 | Mus musculus (house mouse) | 16668 | Krt18 |
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| DOID:0060365 | mandibulofacial dysostosis with alopecia | MGI:105923 | Mus musculus (house mouse) | 13617 | Ednra |
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| DOID:0060041 | autism spectrum disorder | MGI:1915022 | Mus musculus (house mouse) | 67772 | Chd8 |
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| DOID:3827 | congenital diaphragmatic hernia | RGD:69408 | Rattus norvegicus (Norway rat) | 170496 | Lcn2 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:6526 | Homo sapiens (human) | 3934 | LCN2 |
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