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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9538 | multiple myeloma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:418 | systemic scleroderma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:13375 | temporal arteritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:2841 | asthma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:5844 | myocardial infarction | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:1380 | endometrial cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3371 | chondrosarcoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0050771 | pheochromocytoma | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:783 | end stage renal disease | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:10283 | prostate cancer | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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| DOID:10534 | stomach cancer | HGNC:19233 | Homo sapiens (human) | 170384 | FUT11 |
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| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:9884 | muscular dystrophy | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050453 | lissencephaly | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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