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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:418 | systemic scleroderma | HGNC:16647 | Homo sapiens (human) | 10663 | CXCR6 |
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| DOID:9256 | colorectal cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:10534 | stomach cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:3119 | gastrointestinal system cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:3571 | liver cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:0070383 | developmental and epileptic encephalopathy 97 | HGNC:2550 | Homo sapiens (human) | 10659 | CELF2 |
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| DOID:225 | syndrome | MGI:1925212 | Mus musculus (house mouse) | 106583 | Scaf8 |
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| DOID:13608 | biliary atresia | HGNC:11247 | Homo sapiens (human) | 10653 | SPINT2 |
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| DOID:0060781 | congenital secretory sodium diarrhea 3 | HGNC:11247 | Homo sapiens (human) | 10653 | SPINT2 |
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| DOID:0050889 | non-syndromic intellectual disability | MGI:1915408 | Mus musculus (house mouse) | 106529 | Tecr |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | MGI:1915408 | Mus musculus (house mouse) | 106529 | Tecr |
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| DOID:3070 | high grade glioma | HGNC:1470 | Homo sapiens (human) | 10645 | CAMKK2 |
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| DOID:0060158 | acquired metabolic disease | HGNC:28868 | Homo sapiens (human) | 10643 | IGF2BP3 |
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| DOID:0060158 | acquired metabolic disease | HGNC:28866 | Homo sapiens (human) | 10642 | IGF2BP1 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | MGI:2146634 | Mus musculus (house mouse) | 106407 | Slc51a |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | MGI:2146634 | Mus musculus (house mouse) | 106407 | Slc51a |
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| DOID:0110500 | autosomal recessive nonsyndromic deafness 42 | MGI:2146574 | Mus musculus (house mouse) | 106347 | Ildr1 |
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| DOID:6000 | congestive heart failure | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:1474 | aggressive periodontitis | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:783 | end stage renal disease | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:971 | tendinitis | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:90 | degenerative disc disease | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:824 | periodontitis | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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| DOID:5844 | myocardial infarction | HGNC:16953 | Homo sapiens (human) | 10631 | POSTN |
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