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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:2945 | severe acute respiratory syndrome | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:4195 | hyperglycemia | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:1459 | hypothyroidism | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0081101 | nonautoimmune hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0081102 | familial gestational hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:12361 | Graves' disease | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:7998 | hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0050700 | cardiomyopathy | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:988 | mitral valve prolapse | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:9970 | obesity | MGI:1919785 | Mus musculus (house mouse) | 72535 | Aldh1b1 |
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| DOID:684 | hepatocellular carcinoma | MGI:1919815 | Mus musculus (house mouse) | 72565 | Uaca |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | MGI:1919834 | Mus musculus (house mouse) | 72584 | Cul4b |
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| DOID:1059 | intellectual disability | MGI:1919834 | Mus musculus (house mouse) | 72584 | Cul4b |
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| DOID:14227 | azoospermia | MGI:1919884 | Mus musculus (house mouse) | 72634 | Tdrkh |
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| DOID:9538 | multiple myeloma | MGI:1919912 | Mus musculus (house mouse) | 72662 | Dis3 |
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| DOID:5426 | primary ovarian insufficiency | MGI:1919912 | Mus musculus (house mouse) | 72662 | Dis3 |
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| DOID:0060891 | Parkinson's disease 19A | MGI:1919935 | Mus musculus (house mouse) | 72685 | Dnajc6 |
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| DOID:14330 | Parkinson's disease | MGI:1919935 | Mus musculus (house mouse) | 72685 | Dnajc6 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:2841 | asthma | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:8158 | complement component 5 deficiency | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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