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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:1495 | cystic echinococcosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:1059 | intellectual disability | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12711 | Homo sapiens (human) | 9559 | VPS26A |
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| DOID:5750 | endometrial serous adenocarcinoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0111438 | optic atrophy 5 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:0081082 | acute myelomonocytic leukemia | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:0111021 | cone-rod dystrophy 15 | HGNC:14550 | Homo sapiens (human) | 92211 | CDHR1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:0080804 | cranioectodermal dysplasia 2 | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:11656 | cicatricial pemphigoid | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:3500 | gallbladder adenocarcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050871 | fibroma | HGNC:21732 | Homo sapiens (human) | 118429 | ANTXR2 |
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| DOID:11119 | Gilles de la Tourette syndrome | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:0050998 | nonprogressive cerebellar ataxia with mental retardation | HGNC:18806 | Homo sapiens (human) | 23261 | CAMTA1 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | HGNC:13941 | Homo sapiens (human) | 80736 | SLC44A4 |
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| DOID:1417 | choroid disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2701 | Homo sapiens (human) | 1630 | DCC |
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| DOID:1793 | pancreatic cancer | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:9976 | heroin dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:6665 | Homo sapiens (human) | 4016 | LOXL1 |
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| DOID:0080548 | Noonan syndrome with multiple lentigines 1 | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:13564 | aspergillosis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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