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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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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:0070509 | Schinzel Giedion syndrome | MGI:1933199 | Mus musculus (house mouse) | 240427 | Setbp1 |
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| DOID:0070505 | mitochondrial complex IV deficiency nuclear type 20 | RGD:620607 | Rattus norvegicus (Norway rat) | 252934 | Cox5a |
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| DOID:0070505 | mitochondrial complex IV deficiency nuclear type 20 | MGI:88474 | Mus musculus (house mouse) | 12858 | Cox5a |
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| DOID:0070501 | mitochondrial complex IV deficiency nuclear type 16 | MGI:88473 | Mus musculus (house mouse) | 12857 | Cox4i1 |
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| DOID:0070501 | mitochondrial complex IV deficiency nuclear type 16 | RGD:68374 | Rattus norvegicus (Norway rat) | 29445 | Cox4i1 |
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| DOID:0070495 | mitochondrial complex IV deficiency nuclear type 8 | HGNC:24316 | Homo sapiens (human) | 51204 | TACO1 |
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| DOID:0070494 | mitochondrial complex IV deficiency nuclear type 7 | MGI:107460 | Mus musculus (house mouse) | 110323 | Cox6b1 |
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| DOID:0070491 | mitochondrial complex IV deficiency nuclear type 1 | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:0070490 | infantile parkinsonism-dystonia 2 | MGI:106677 | Mus musculus (house mouse) | 214084 | Slc18a2 |
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| DOID:0070490 | infantile parkinsonism-dystonia 2 | HGNC:10935 | Homo sapiens (human) | 6571 | SLC18A2 |
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| DOID:0070490 | infantile parkinsonism-dystonia 2 | RGD:3694 | Rattus norvegicus (Norway rat) | 25549 | Slc18a2 |
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| DOID:0070490 | infantile parkinsonism-dystonia 2 | WB:WBGene00000295 | Caenorhabditis elegans | 180837 | cat-1 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | WB:WBGene00000934 | Caenorhabditis elegans | 176304 | dat-1 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | HGNC:11049 | Homo sapiens (human) | 6531 | SLC6A3 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | FB:FBgn0034136 | Drosophila melanogaster (fruit fly) | 36849 | DAT |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | MGI:1270850 | Mus musculus (house mouse) | 20538 | Slc6a2 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | MGI:94862 | Mus musculus (house mouse) | 13162 | Slc6a3 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | RGD:3715 | Rattus norvegicus (Norway rat) | 24898 | Slc6a3 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:0070486 | Parkinson's disease 25 | HGNC:9308 | Homo sapiens (human) | 5524 | PTPA |
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| DOID:0070486 | Parkinson's disease 25 | MGI:1346006 | Mus musculus (house mouse) | 110854 | Ptpa |
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| DOID:0070485 | mitochondrial complex IV deficiency nuclear type 23 | HGNC:2261 | Homo sapiens (human) | 1353 | COX11 |
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| DOID:0070484 | Legius syndrome | MGI:2150016 | Mus musculus (house mouse) | 114715 | Spred1 |
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| DOID:0070484 | Legius syndrome | HGNC:20249 | Homo sapiens (human) | 161742 | SPRED1 |
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| DOID:0070483 | Watson syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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