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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:684 | hepatocellular carcinoma | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:11266 | Hantavirus hemorrhagic fever with renal syndrome | HGNC:4953 | Homo sapiens (human) | 3127 | HLA-DRB5 |
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| DOID:9008 | psoriatic arthritis | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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| DOID:1561 | cognitive disorder | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:1574 | alcohol use disorder | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:6181 | Homo sapiens (human) | 3709 | ITPR2 |
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| DOID:10126 | keratoconus | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0111353 | arthrogryposis, renal dysfunction, and cholestasis 1 | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
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| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9975 | cocaine dependence | HGNC:17025 | Homo sapiens (human) | 81578 | COL21A1 |
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| DOID:0080980 | arthrogryposis multiplex congenita-4 | HGNC:19286 | Homo sapiens (human) | 55681 | SCYL2 |
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| DOID:2841 | asthma | HGNC:4947 | Homo sapiens (human) | 3122 | HLA-DRA |
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| DOID:0111637 | autosomal recessive nonsyndromic deafness 112 | HGNC:13652 | Homo sapiens (human) | 55814 | BDP1 |
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| DOID:8893 | psoriasis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0111620 | corneal dystrophy-perceptive deafness syndrome | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
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| DOID:0111853 | primary ciliary dyskinesia 40 | HGNC:2953 | Homo sapiens (human) | 1770 | DNAH9 |
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| DOID:0080600 | COVID-19 | HGNC:1328 | Homo sapiens (human) | 725 | C4BPB |
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| DOID:1380 | endometrial cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:13375 | temporal arteritis | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:13316 | exocrine pancreatic insufficiency | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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