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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
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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:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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| DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:11727 | facioscapulohumeral muscular dystrophy | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:162 | cancer | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:12662 | paracoccidioidomycosis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:874 | bacterial pneumonia | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:3393 | coronary artery disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:9408 | acute myocardial infarction | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:11266 | Hantavirus hemorrhagic fever with renal syndrome | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:4483 | rhinitis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:2841 | asthma | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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