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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:1390 | hypobetalipoproteinemia | HGNC:20001 | Homo sapiens (human) | 255738 | PCSK9 |
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| DOID:0081359 | epidermolytic hyperkeratosis 2 | HGNC:6413 | Homo sapiens (human) | 3858 | KRT10 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0050453 | lissencephaly | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:2043 | hepatitis B | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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| DOID:11758 | iron deficiency anemia | HGNC:11740 | Homo sapiens (human) | 7018 | TF |
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| DOID:0110732 | neuronal ceroid lipofuscinosis 11 | HGNC:4601 | Homo sapiens (human) | 2896 | GRN |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:0111952 | immunodeficiency 57 | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:0081289 | Antley-Bixler syndrome | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:0070483 | Watson syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:6364 | migraine | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:0080334 | aortic valve disease 2 | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:9119 | acute myeloid leukemia | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:0070529 | Sifrim-Hitz-Weiss syndrome | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:4481 | allergic rhinitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11162 | respiratory failure | HGNC:17859 | Homo sapiens (human) | 23511 | NUP188 |
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| DOID:5082 | liver cirrhosis | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:0110428 | dilated cardiomyopathy 1AA | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:0080600 | COVID-19 | HGNC:1325 | Homo sapiens (human) | 722 | C4BPA |
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