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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1596 | depressive disorder | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:6543 | acne | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8893 | psoriasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:874 | bacterial pneumonia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:14749 | methylmalonic acidemia | HGNC:16732 | Homo sapiens (human) | 84693 | MCEE |
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| DOID:784 | chronic kidney disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:10787 | premature menopause | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
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| DOID:1508 | candidiasis | RGD:619955 | Rattus norvegicus (Norway rat) | 84597 | Fut9 |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | RGD:620355 | Rattus norvegicus (Norway rat) | 84468 | Chst3 |
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| DOID:2256 | osteochondrodysplasia | RGD:620355 | Rattus norvegicus (Norway rat) | 84468 | Chst3 |
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| DOID:5419 | schizophrenia | RGD:620355 | Rattus norvegicus (Norway rat) | 84468 | Chst3 |
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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:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0050700 | cardiomyopathy | 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:9296 | cleft lip | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:0050453 | lissencephaly | 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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