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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:0112202 | developmental and epileptic encephalopathy | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:0080436 | developmental and epileptic encephalopathy 4 | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:0050709 | early infantile epileptic encephalopathy | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:0050562 | West syndrome | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:1826 | epilepsy | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:11445 | Homo sapiens (human) | 6813 | STXBP2 |
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| DOID:1574 | alcohol use disorder | HGNC:11445 | Homo sapiens (human) | 6813 | STXBP2 |
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| DOID:0110925 | familial hemophagocytic lymphohistiocytosis 5 | HGNC:11445 | Homo sapiens (human) | 6813 | STXBP2 |
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| DOID:0112139 | nuclear type mitochondrial complex I deficiency 35 | RGD:1310782 | Rattus norvegicus (Norway rat) | 681418 | Ndufb10 |
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| DOID:0111003 | Joubert syndrome 8 | MGI:1915396 | Mus musculus (house mouse) | 68146 | Arl13b |
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| DOID:0111903 | thrombophilia due to HRG deficiency | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrgl1 |
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| DOID:0060903 | thrombosis | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrg l1 |
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| DOID:0060903 | thrombosis | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrgl1 |
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| DOID:4074 | pancreatic adenocarcinoma | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrg l1 |
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| DOID:0111903 | thrombophilia due to HRG deficiency | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrg l1 |
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| DOID:4074 | pancreatic adenocarcinoma | RGD:1594092 | Rattus norvegicus (Norway rat) | 681544 | Hrgl1 |
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| DOID:0112209 | developmental and epileptic encephalopathy 73 | RGD:1594062 | Rattus norvegicus (Norway rat) | 681578 | Rnf13 |
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| DOID:0090070 | hypogonadotropic hypogonadism | MGI:1915419 | Mus musculus (house mouse) | 68169 | Ndnf |
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| DOID:0110704 | hypotrichosis 7 | RGD:1592849 | Rattus norvegicus (Norway rat) | 681694 | Liph |
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| DOID:1612 | breast cancer | MGI:1915433 | Mus musculus (house mouse) | 68183 | Bcas2 |
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| DOID:5410 | pulmonary neuroendocrine tumor | MGI:3702087 | Mus musculus (house mouse) | 68195 | Rnaset2b |
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| DOID:0081007 | RNASET2-deficient cystic leukoencephalopathy | MGI:3702087 | Mus musculus (house mouse) | 68195 | Rnaset2b |
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| DOID:234 | colon adenocarcinoma | MGI:3702087 | Mus musculus (house mouse) | 68195 | Rnaset2b |
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| DOID:0112182 | mismatch repair cancer syndrome | MGI:3702087 | Mus musculus (house mouse) | 68195 | Rnaset2b |
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| DOID:3717 | gastric adenocarcinoma | MGI:3702087 | Mus musculus (house mouse) | 68195 | Rnaset2b |
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