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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:8398 | osteoarthritis | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:0070441 | retinal macular dystrophy 4 | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7148 | rheumatoid arthritis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:1289 | neurodegenerative disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:2377 | multiple sclerosis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:0112162 | autosomal recessive nonsyndromic deafness 116 | HGNC:2051 | Homo sapiens (human) | 9080 | CLDN9 |
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| DOID:9778 | irritable bowel syndrome | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:5082 | liver cirrhosis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:3310 | atopic dermatitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:824 | periodontitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:8778 | Crohn's disease | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:687 | hepatoblastoma | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:8947 | diabetic retinopathy | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:0110146 | Bartter disease type 4b | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:445 | Bartter disease | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:423 | myopathy | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0110144 | Bartter disease type 3 | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0050450 | Gitelman syndrome | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:10763 | hypertension | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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