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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:12858 | Huntington's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:219 | colon cancer | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:1612 | breast cancer | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:13580 | cholestasis | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:3908 | lung non-small cell carcinoma | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:14330 | Parkinson's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:9970 | obesity | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:3534 | Lafora disease | MGI:2145264 | Mus musculus (house mouse) | 105193 | Nhlrc1 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:162 | cancer | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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