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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:0050588 | muscular dystrophy-dystroglycanopathy type B1 | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:150 | disease of mental health | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:783 | end stage renal disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:1184 | nephrotic syndrome | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:10908 | hydrocephalus | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:11446 | sciatic neuropathy | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:332 | amyotrophic lateral sclerosis | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:3312 | bipolar disorder | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:5419 | schizophrenia | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:219 | colon cancer | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:114 | heart disease | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:90 | degenerative disc disease | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:9408 | acute myocardial infarction | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:2871 | endometrial carcinoma | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:10652 | Alzheimer's disease | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
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| DOID:8725 | vascular dementia | RGD:70982 | Rattus norvegicus (Norway rat) | 84027 | Gsk3b |
|
