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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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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:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:14723 | beta-ketothiolase deficiency | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:14717 | centronuclear myopathy | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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| DOID:14717 | centronuclear myopathy | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
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| DOID:14717 | centronuclear myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:14717 | centronuclear myopathy | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:14701 | propionic acidemia | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:1470 | major depressive disorder | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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| DOID:1470 | major depressive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:1470 | major depressive disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:1470 | major depressive disorder | MGI:109521 | Mus musculus (house mouse) | 15558 | Htr2a |
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| DOID:14695 | galactokinase deficiency | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:14695 | galactokinase deficiency | MGI:95730 | Mus musculus (house mouse) | 14635 | Galk1 |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:14687 | diastrophic dysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:14681 | Silver-Russell syndrome | MGI:96434 | Mus musculus (house mouse) | 16002 | Igf2 |
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| DOID:14681 | Silver-Russell syndrome | RGD:2870 | Rattus norvegicus (Norway rat) | 24483 | Igf2 |
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| DOID:14681 | Silver-Russell syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:14654 | prostatitis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:14654 | prostatitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1459 | hypothyroidism | MGI:1096330 | Mus musculus (house mouse) | 12015 | Bad |
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| DOID:1459 | hypothyroidism | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:1459 | hypothyroidism | Xenbase:XB-GENE-5916631 | Xenopus tropicalis (tropical clawed frog) | 734090 | plod3 |
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| DOID:1459 | hypothyroidism | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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