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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:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:1289 | neurodegenerative disease | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:231 | motor neuron disease | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:0050752 | amyotrophic lateral sclerosis type 8 | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:12377 | spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:1289 | neurodegenerative disease | HGNC:12648 | Homo sapiens (human) | 9218 | VAPA |
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| DOID:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12648 | Homo sapiens (human) | 9218 | VAPA |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:12648 | Homo sapiens (human) | 9218 | VAPA |
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| DOID:231 | motor neuron disease | HGNC:12648 | Homo sapiens (human) | 9218 | VAPA |
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| DOID:0050752 | amyotrophic lateral sclerosis type 8 | HGNC:12648 | Homo sapiens (human) | 9218 | VAPA |
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| DOID:2908 | Treacher Collins syndrome | HGNC:15608 | Homo sapiens (human) | 9221 | NOLC1 |
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| DOID:0111021 | cone-rod dystrophy 15 | HGNC:14550 | Homo sapiens (human) | 92211 | CDHR1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:9761 | Homo sapiens (human) | 9230 | RAB11B |
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| DOID:10155 | intestinal cancer | HGNC:9761 | Homo sapiens (human) | 9230 | RAB11B |
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| DOID:0070511 | polyhydramnios, megalencephaly, and symptomatic epilepsy | HGNC:30172 | Homo sapiens (human) | 92335 | STRADA |
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| DOID:1826 | epilepsy | HGNC:30172 | Homo sapiens (human) | 92335 | STRADA |
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| DOID:0080171 | esophageal atresia/tracheoesophageal fistula | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:9296 | cleft lip | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:12858 | Huntington's disease | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:0050788 | proximal symphalangism | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:0081317 | multiple synostoses syndrome 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:9834 | hyperopia | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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