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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:0060688 | arteriovenous malformations of the brain | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:17938 | Homo sapiens (human) | 50632 | CALY |
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| DOID:0050469 | Costello syndrome | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:6000 | congestive heart failure | HGNC:7166 | Homo sapiens (human) | 4313 | MMP2 |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:1612 | breast cancer | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:1596 | depressive disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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| DOID:10763 | hypertension | RGD:2535 | Rattus norvegicus (Norway rat) | 24326 | Ednra |
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| DOID:0060291 | oculodentodigital dysplasia | MGI:95713 | Mus musculus (house mouse) | 14609 | Gja1 |
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| DOID:0110871 | congenital stationary night blindness 2A | MGI:1859639 | Mus musculus (house mouse) | 54652 | Cacna1f |
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| DOID:10763 | hypertension | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:1826 | epilepsy | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
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| DOID:10907 | microcephaly | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:10763 | hypertension | HGNC:9958 | Homo sapiens (human) | 5972 | REN |
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| DOID:1574 | alcohol use disorder | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:289 | endometriosis | HGNC:8910 | Homo sapiens (human) | 5241 | PGR |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:12387 | nephrogenic diabetes insipidus | MGI:1096865 | Mus musculus (house mouse) | 11827 | Aqp2 |
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| DOID:4483 | rhinitis | HGNC:10610 | Homo sapiens (human) | 6356 | CCL11 |
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| DOID:5844 | myocardial infarction | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:9452 | steatotic liver disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:13515 | tuberous sclerosis | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:13515 | tuberous sclerosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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