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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:0090001 | Fraser syndrome | MGI:2444465 | Mus musculus (house mouse) | 242022 | Frem2 |
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| DOID:0111789 | Frank-Ter Haar syndrome | HGNC:29242 | Homo sapiens (human) | 285590 | SH3PXD2B |
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| DOID:0111789 | Frank-Ter Haar syndrome | MGI:2442062 | Mus musculus (house mouse) | 268396 | Sh3pxd2b |
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| DOID:0111358 | Floating-Harbor syndrome | HGNC:16974 | Homo sapiens (human) | 10847 | SRCAP |
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| DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0060448 | Fleck corneal dystrophy | SGD:S000001915 | Saccharomyces cerevisiae S288C | 850574 | FAB1 |
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| DOID:0050637 | Finnish type amyloidosis | HGNC:4620 | Homo sapiens (human) | 2934 | GSN |
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| DOID:0050637 | Finnish type amyloidosis | MGI:95851 | Mus musculus (house mouse) | 227753 | Gsn |
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| DOID:0112194 | Filippi syndrome | HGNC:26877 | Homo sapiens (human) | 150468 | CKAP2L |
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| DOID:0112194 | Filippi syndrome | MGI:1917716 | Mus musculus (house mouse) | 70466 | Ckap2l |
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| DOID:5585 | Ferguson-Smith tumor | WB:WBGene00004860 | Caenorhabditis elegans | 174044 | sma-6 |
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| DOID:5585 | Ferguson-Smith tumor | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:5585 | Ferguson-Smith tumor | MGI:98728 | Mus musculus (house mouse) | 21812 | Tgfbr1 |
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| DOID:5585 | Ferguson-Smith tumor | WB:WBGene00000897 | Caenorhabditis elegans | 176829 | daf-1 |
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| DOID:5585 | Ferguson-Smith tumor | RGD:3852 | Rattus norvegicus (Norway rat) | 29591 | Tgfbr1 |
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| DOID:0060464 | Feingold syndrome | MGI:97357 | Mus musculus (house mouse) | 18109 | Mycn |
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| DOID:0060464 | Feingold syndrome | HGNC:7559 | Homo sapiens (human) | 4613 | MYCN |
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| DOID:0080632 | Fazio-Londe disease | MGI:1916948 | Mus musculus (house mouse) | 69698 | Slc52a3 |
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| DOID:0080632 | Fazio-Londe disease | RGD:1304644 | Rattus norvegicus (Norway rat) | 311536 | Slc52a3 |
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| DOID:0080632 | Fazio-Londe disease | WB:WBGene00021626 | Caenorhabditis elegans | 178842 | rft-2 |
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| DOID:0080632 | Fazio-Londe disease | ZFIN:ZDB-GENE-060421-4490 | Danio rerio (zebrafish) | 678609 | slc52a3-1 |
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| DOID:0080632 | Fazio-Londe disease | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0050464 | Farber lipogranulomatosis | RGD:621568 | Rattus norvegicus (Norway rat) | 84431 | Asah1 |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0050464 | Farber lipogranulomatosis | WB:WBGene00009192 | Caenorhabditis elegans | 185021 | asah-2 |
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