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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:3320 | Tay-Sachs disease | RGD:2792 | Rattus norvegicus (Norway rat) | 300757 | Hexa |
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| DOID:0080554 | congenital disorder of glycosylation Ib | RGD:3107 | Rattus norvegicus (Norway rat) | 300741 | Mpi |
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| DOID:0050570 | congenital disorder of glycosylation type I | RGD:3107 | Rattus norvegicus (Norway rat) | 300741 | Mpi |
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| DOID:2978 | carbohydrate metabolic disorder | RGD:3107 | Rattus norvegicus (Norway rat) | 300741 | Mpi |
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| DOID:0080562 | congenital disorder of glycosylation Ij | RGD:735124 | Rattus norvegicus (Norway rat) | 300668 | Dpagt1 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | RGD:735124 | Rattus norvegicus (Norway rat) | 300668 | Dpagt1 |
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| DOID:0111156 | spermatogenic failure 9 | RGD:1564311 | Rattus norvegicus (Norway rat) | 300461 | Dpy19l2 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | RGD:1359416 | Rattus norvegicus (Norway rat) | 300284 | Alg13l1 |
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| DOID:206 | hereditary multiple exostoses | RGD:1587375 | Rattus norvegicus (Norway rat) | 299907 | Ext1 |
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| DOID:0060041 | autism spectrum disorder | RGD:1587375 | Rattus norvegicus (Norway rat) | 299907 | Ext1 |
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| DOID:3371 | chondrosarcoma | RGD:1587375 | Rattus norvegicus (Norway rat) | 299907 | Ext1 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:1309356 | Rattus norvegicus (Norway rat) | 299841 | Rxylt1 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | RGD:1309356 | Rattus norvegicus (Norway rat) | 299841 | Rxylt1 |
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| DOID:3534 | Lafora disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:3534 | Lafora disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:0111141 | delayed sleep phase syndrome | RGD:735083 | Rattus norvegicus (Norway rat) | 299691 | Cry1 |
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| DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:9884 | muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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