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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:0070011 | Seckel syndrome 7 | HGNC:14906 | Homo sapiens (human) | 51199 | NIN |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:14218 | dihydropyrimidine dehydrogenase deficiency | HGNC:3012 | Homo sapiens (human) | 1806 | DPYD |
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| DOID:10652 | Alzheimer's disease | HGNC:6367 | Homo sapiens (human) | 5653 | KLK6 |
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| DOID:8997 | polycythemia vera | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:5082 | liver cirrhosis | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:12029 | sympathetic ophthalmia | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111452 | progressive myoclonus epilepsy 1A | HGNC:2482 | Homo sapiens (human) | 1476 | CSTB |
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| DOID:11165 | common wart | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:3082 | interstitial lung disease | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:6713 | cerebrovascular disease | HGNC:18124 | Homo sapiens (human) | 64805 | P2RY12 |
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| DOID:0081317 | multiple synostoses syndrome 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:4481 | allergic rhinitis | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:8947 | diabetic retinopathy | HGNC:25156 | Homo sapiens (human) | 112869 | SGF29 |
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| DOID:4079 | heart valve disease | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0111193 | facioscapulohumeral muscular dystrophy 2 | HGNC:29090 | Homo sapiens (human) | 23347 | SMCHD1 |
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| DOID:4377 | egg allergy | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:1380 | endometrial cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:9279 | Homo sapiens (human) | 54704 | PDP1 |
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| DOID:0111504 | Li-Fraumeni syndrome 2 | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:12241 | beta thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1205 | allergic disease | HGNC:7097 | Homo sapiens (human) | 4282 | MIF |
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| DOID:0070164 | spermatogenic failure 2 | HGNC:7327 | Homo sapiens (human) | 4438 | MSH4 |
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| DOID:0070135 | autosomal recessive cutis laxa type IA | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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