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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:0080913 | cerebrooculofacioskeletal syndrome 3 | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0111911 | spermatogenic failure 34 | HGNC:21675 | Homo sapiens (human) | 401024 | FSIP2 |
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| DOID:5082 | liver cirrhosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10825 | essential hypertension | HGNC:9642 | Homo sapiens (human) | 5770 | PTPN1 |
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| DOID:0110705 | hypotrichosis 8 | HGNC:15520 | Homo sapiens (human) | 10161 | LPAR6 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10652 | Alzheimer's disease | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:12306 | vitiligo | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0080978 | arthrogryposis multiplex congenita-1 | HGNC:18712 | Homo sapiens (human) | 163175 | LGI4 |
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| DOID:0060488 | Pitt-Hopkins syndrome | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:1024 | leprosy | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:13375 | temporal arteritis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110348 | osteogenesis imperfecta type 12 | HGNC:17321 | Homo sapiens (human) | 121340 | SP7 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:9206 | Barrett's esophagus | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:2224 | essential thrombocythemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:8466 | retinal degeneration | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0081030 | central conducting lymphatic anomaly | HGNC:3395 | Homo sapiens (human) | 2050 | EPHB4 |
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| DOID:0081203 | autosomal recessive intellectual developmental disorder 38 | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:12134 | factor VIII deficiency | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0111391 | mucopolysaccharidosis IVA | HGNC:4122 | Homo sapiens (human) | 2588 | GALNS |
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| DOID:7148 | rheumatoid arthritis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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