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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:3068 | glioblastoma | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:4914 | esophagus adenocarcinoma | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:1612 | breast cancer | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:9352 | type 2 diabetes mellitus | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:2377 | multiple sclerosis | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:684 | hepatocellular carcinoma | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:3070 | high grade glioma | MGI:88561 | Mus musculus (house mouse) | 13030 | Ctsb |
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| DOID:0050663 | Bethlem myopathy | HGNC:2188 | Homo sapiens (human) | 1303 | COL12A1 |
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| DOID:674 | cleft palate | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080026 | otospondylomegaepiphyseal dysplasia, autosomal recessive | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080673 | fibrochondrogenesis 2 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080677 | otospondylomegaepiphyseal dysplasia, autosomal dominant | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:1574 | alcohol use disorder | MGI:1201685 | Mus musculus (house mouse) | 13016 | Ctbp1 |
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| DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:2913 | acute pancreatitis | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:552 | pneumonia | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:3393 | coronary artery disease | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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| DOID:341 | peripheral vascular disease | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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