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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080575 | Larsen-like syndrome B3GAT3 type | HGNC:923 | Homo sapiens (human) | 26229 | B3GAT3 |
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| DOID:0050636 | familial visceral amyloidosis | HGNC:6740 | Homo sapiens (human) | 4069 | LYZ |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1496 | echinococcosis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:2043 | hepatitis B | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:594 | panic disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:0080108 | myoglobinuria | HGNC:8889 | Homo sapiens (human) | 5224 | PGAM2 |
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| DOID:9975 | cocaine dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:5517 | stomach carcinoma | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:9970 | obesity | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:0050598 | extrapulmonary tuberculosis | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:3500 | gallbladder adenocarcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9146 | visceral leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:2256 | osteochondrodysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:74 | hematopoietic system disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:14330 | Parkinson's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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