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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:0050474 | Netherton syndrome | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:26789 | Homo sapiens (human) | 144811 | LACC1 |
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| DOID:0080201 | Peters plus syndrome | HGNC:20207 | Homo sapiens (human) | 145173 | B3GLCT |
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| DOID:11716 | prediabetes syndrome | MGI:95674 | Mus musculus (house mouse) | 14526 | Gcg |
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| DOID:10652 | Alzheimer's disease | MGI:95674 | Mus musculus (house mouse) | 14526 | Gcg |
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| DOID:9970 | obesity | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:13372 | alpha 1-antitrypsin deficiency | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:114 | heart disease | MGI:1343101 | Mus musculus (house mouse) | 14534 | Kat2a |
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| DOID:557 | kidney disease | MGI:1343101 | Mus musculus (house mouse) | 14534 | Kat2a |
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| DOID:3908 | lung non-small cell carcinoma | MGI:1343101 | Mus musculus (house mouse) | 14534 | Kat2a |
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| DOID:83 | cataract | MGI:1100870 | Mus musculus (house mouse) | 14538 | Gcnt2 |
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| DOID:0110242 | cataract 13 with adult i phenotype | MGI:1100870 | Mus musculus (house mouse) | 14538 | Gcnt2 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:99778 | Mus musculus (house mouse) | 14571 | Gpd2 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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| DOID:2986 | IgA glomerulonephritis | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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| DOID:28 | endocrine system disease | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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| DOID:5212 | congenital disorder of glycosylation | MGI:95705 | Mus musculus (house mouse) | 14595 | B4galt1 |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:5844 | myocardial infarction | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:10941 | intracranial aneurysm | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:0060363 | glycerol kinase deficiency | MGI:1329027 | Mus musculus (house mouse) | 14626 | Gk2 |
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| DOID:9675 | pulmonary emphysema | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:5844 | myocardial infarction | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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| DOID:1485 | cystic fibrosis | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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