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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: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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| 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: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:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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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: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:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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| DOID:1826 | epilepsy | HGNC:1400 | Homo sapiens (human) | 9254 | CACNA2D2 |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1485 | cystic fibrosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13608 | biliary atresia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10763 | hypertension | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2841 | asthma | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:4483 | rhinitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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