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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:11476 | osteoporosis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:2349 | arteriosclerosis | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:5585 | Ferguson-Smith tumor | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:11476 | osteoporosis | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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| DOID:399 | tuberculosis | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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| DOID:2841 | asthma | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:0080380 | nephrotic syndrome type 5 | HGNC:6487 | Homo sapiens (human) | 3913 | LAMB2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0060464 | Feingold syndrome | HGNC:7559 | Homo sapiens (human) | 4613 | MYCN |
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| DOID:409 | liver disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3121 | gallbladder cancer | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:0050656 | pseudo-TORCH syndrome 1 | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:10123 | pigmentation disease | HGNC:20820 | Homo sapiens (human) | 219931 | TPCN2 |
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| DOID:1485 | cystic fibrosis | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8973 | Homo sapiens (human) | 5288 | PIK3C2G |
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| DOID:9538 | multiple myeloma | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:612 | primary immunodeficiency disease | HGNC:6024 | Homo sapiens (human) | 3575 | IL7R |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:2218 | blood platelet disease | HGNC:12013 | Homo sapiens (human) | 7171 | TPM4 |
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| DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0060181 | ischemic colitis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0110813 | hereditary spastic paraplegia 62 | HGNC:16947 | Homo sapiens (human) | 10613 | ERLIN1 |
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| DOID:0080745 | polymyositis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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