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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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MIRAGE
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:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0080108 | myoglobinuria | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:9970 | obesity | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:0060037 | developmental disorder of mental health | HGNC:14454 | Homo sapiens (human) | 55879 | GABRQ |
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||
| DOID:1826 | epilepsy | HGNC:14465 | Homo sapiens (human) | 89822 | KCNK17 |
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| DOID:10273 | heart conduction disease | HGNC:14465 | Homo sapiens (human) | 89822 | KCNK17 |
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| DOID:114 | heart disease | HGNC:14465 | Homo sapiens (human) | 89822 | KCNK17 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:14467 | Homo sapiens (human) | 115111 | SLC26A7 |
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| DOID:0070168 | spermatogenic failure 3 | HGNC:14468 | Homo sapiens (human) | 116369 | SLC26A8 |
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| DOID:0111473 | combined oxidative phosphorylation deficiency 5 | HGNC:14508 | Homo sapiens (human) | 56945 | MRPS22 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:14508 | Homo sapiens (human) | 56945 | MRPS22 |
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| DOID:0080499 | ovarian dysgenesis 7 | HGNC:14508 | Homo sapiens (human) | 56945 | MRPS22 |
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| DOID:0112115 | combined oxidative phosphorylation deficiency 46 | HGNC:14509 | Homo sapiens (human) | 51649 | MRPS23 |
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| DOID:5082 | liver cirrhosis | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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| DOID:684 | hepatocellular carcinoma | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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| DOID:1380 | endometrial cancer | HGNC:14524 | Homo sapiens (human) | 9043 | SPAG9 |
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| DOID:14504 | Niemann-Pick disease | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
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| DOID:0070114 | Niemann-Pick disease type C2 | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
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| DOID:13099 | Moyamoya disease | HGNC:14539 | Homo sapiens (human) | 57674 | RNF213 |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:14539 | Homo sapiens (human) | 57674 | RNF213 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:224 | transient cerebral ischemia | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:10763 | hypertension | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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