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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:0050453 | lissencephaly | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:9296 | cleft lip | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:9884 | muscular dystrophy | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:1927 | sphingolipidosis | RGD:621568 | Rattus norvegicus (Norway rat) | 84431 | Asah1 |
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| DOID:0050464 | Farber lipogranulomatosis | RGD:621568 | Rattus norvegicus (Norway rat) | 84431 | Asah1 |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | RGD:621568 | Rattus norvegicus (Norway rat) | 84431 | Asah1 |
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| DOID:0111957 | immunodeficiency 11A | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:5603 | T-cell acute lymphoblastic leukemia | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:0111958 | immunodeficiency 11B | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:0110425 | dilated cardiomyopathy 1A | HGNC:24948 | Homo sapiens (human) | 84444 | DOT1L |
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| DOID:0050888 | syndromic intellectual disability | HGNC:24948 | Homo sapiens (human) | 84444 | DOT1L |
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| DOID:9953 | acute biphenotypic leukemia | HGNC:24948 | Homo sapiens (human) | 84444 | DOT1L |
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| DOID:1240 | leukemia | HGNC:24948 | Homo sapiens (human) | 84444 | DOT1L |
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| DOID:18 | urinary system disease | HGNC:29381 | Homo sapiens (human) | 84445 | LZTS2 |
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| DOID:13372 | alpha 1-antitrypsin deficiency | HGNC:20738 | Homo sapiens (human) | 84447 | SYVN1 |
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| DOID:1289 | neurodegenerative disease | HGNC:29635 | Homo sapiens (human) | 84465 | MEGF11 |
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| DOID:423 | myopathy | HGNC:29635 | Homo sapiens (human) | 84465 | MEGF11 |
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| DOID:0081345 | congenital myopathy 10B | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
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| DOID:0111333 | early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
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| DOID:423 | myopathy | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
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