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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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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:10763 | hypertension | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:10652 | Alzheimer's disease | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:1574 | alcohol use disorder | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:13580 | cholestasis | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:9351 | diabetes mellitus | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:535 | sleep disorder | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:3312 | bipolar disorder | MGI:99698 | Mus musculus (house mouse) | 12753 | Clock |
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| DOID:14503 | neuronal ceroid lipofuscinosis | MGI:107537 | Mus musculus (house mouse) | 12752 | Cln3 |
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| DOID:0110721 | neuronal ceroid lipofuscinosis 1 | MGI:107537 | Mus musculus (house mouse) | 12752 | Cln3 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | MGI:107537 | Mus musculus (house mouse) | 12752 | Cln3 |
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| DOID:0080059 | autosomal recessive spinocerebellar ataxia 7 | MGI:1336194 | Mus musculus (house mouse) | 12751 | Tpp1 |
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| DOID:0110726 | neuronal ceroid lipofuscinosis 2 | MGI:1336194 | Mus musculus (house mouse) | 12751 | Tpp1 |
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| DOID:10763 | hypertension | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:0110144 | Bartter disease type 3 | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:12387 | nephrogenic diabetes insipidus | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:0050450 | Gitelman syndrome | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:10003 | sensorineural hearing loss | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:423 | myopathy | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:0110146 | Bartter disease type 4b | MGI:1329026 | Mus musculus (house mouse) | 12733 | Clcnka |
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| DOID:447 | renal tubular transport disease | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0050699 | Dent disease | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0111798 | X-linked nephrolithiasis type I | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:13533 | osteopetrosis | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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