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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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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:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:3211 | lysosomal storage disease | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:0080055 | achondrogenesis type IB | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:10652 | Alzheimer's disease | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:552 | pneumonia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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| DOID:2256 | osteochondrodysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:1712 | aortic valve stenosis | RGD:2555 | Rattus norvegicus (Norway rat) | 25438 | Eno3 |
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| DOID:1909 | melanoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9538 | multiple myeloma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:4195 | hyperglycemia | RGD:3336 | Rattus norvegicus (Norway rat) | 24651 | Pklr |
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| DOID:3770 | pulmonary fibrosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:0050685 | small cell carcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:3393 | coronary artery disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:8791 | breast carcinoma in situ | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:8719 | in situ carcinoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:700 | mitochondrial metabolism disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:9256 | colorectal cancer | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:2921 | glomerulonephritis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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