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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
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:0050331 | lacrimoauriculodentodigital syndrome 1 | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:1682 | congenital heart disease | HGNC:6188 | Homo sapiens (human) | 182 | JAG1 |
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| DOID:0110883 | inflammatory bowel disease 17 | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:3507 | dermatofibrosarcoma protuberans | HGNC:8800 | Homo sapiens (human) | 5155 | PDGFB |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:6953 | Homo sapiens (human) | 4179 | CD46 |
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| DOID:0070136 | autosomal dominant cutis laxa 2 | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0070119 | Meckel syndrome 5 | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1957 | Homo sapiens (human) | 1136 | CHRNA3 |
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| DOID:3070 | high grade glioma | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:0060560 | lethal congenital contracture syndrome 2 | HGNC:3431 | Homo sapiens (human) | 2065 | ERBB3 |
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| DOID:2582 | acatalasia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:2841 | asthma | HGNC:7512 | Homo sapiens (human) | 4583 | MUC2 |
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| DOID:13550 | angle-closure glaucoma | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:1059 | intellectual disability | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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| DOID:2377 | multiple sclerosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:7508 | Homo sapiens (human) | 4582 | MUC1 |
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| DOID:4810 | cerebrotendinous xanthomatosis | HGNC:2605 | Homo sapiens (human) | 1593 | CYP27A1 |
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| DOID:12858 | Huntington's disease | HGNC:7996 | Homo sapiens (human) | 4899 | NRF1 |
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| DOID:1793 | pancreatic cancer | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:1612 | breast cancer | HGNC:975 | Homo sapiens (human) | 10286 | BCAS2 |
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| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0110982 | Joubert syndrome 13 | HGNC:26113 | Homo sapiens (human) | 79600 | TCTN1 |
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| DOID:0070038 | autosomal dominant intellectual developmental disorder 8 | HGNC:4584 | Homo sapiens (human) | 2902 | GRIN1 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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