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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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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:0080750 | erythema nodosum | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:10763 | hypertension | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0081318 | multiple synostoses syndrome 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:2841 | asthma | HGNC:4951 | Homo sapiens (human) | 3125 | HLA-DRB3 |
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| DOID:9256 | colorectal cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:9208 | Homo sapiens (human) | 5447 | POR |
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| DOID:2256 | osteochondrodysplasia | HGNC:21317 | Homo sapiens (human) | 54808 | DYM |
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| DOID:0112184 | thyroid dyshormonogenesis 5 | HGNC:32698 | Homo sapiens (human) | 405753 | DUOXA2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7406 | Homo sapiens (human) | 4502 | MT2A |
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| DOID:0111524 | autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | HGNC:11992 | Homo sapiens (human) | 7156 | TOP3A |
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| DOID:0050700 | cardiomyopathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:1059 | intellectual disability | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:3393 | coronary artery disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:0050700 | cardiomyopathy | HGNC:3057 | Homo sapiens (human) | 1837 | DTNA |
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| DOID:5409 | lung small cell carcinoma | HGNC:17675 | Homo sapiens (human) | 57510 | XPO5 |
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| DOID:10123 | pigmentation disease | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:8577 | ulcerative colitis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:3526 | cerebral infarction | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0060746 | basal laminar drusen | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:612 | primary immunodeficiency disease | HGNC:29002 | Homo sapiens (human) | 23149 | FCHO1 |
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| DOID:13099 | Moyamoya disease | HGNC:14539 | Homo sapiens (human) | 57674 | RNF213 |
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| DOID:10763 | hypertension | HGNC:7945 | Homo sapiens (human) | 4883 | NPR3 |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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