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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:2394 | ovarian cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:1793 | pancreatic cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:4897 | bile duct carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:1927 | sphingolipidosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:714 | Homo sapiens (human) | 411 | ARSB |
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| DOID:1459 | hypothyroidism | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7056 | Homo sapiens (human) | 10724 | OGA |
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| DOID:576 | proteinuria | HGNC:7049 | Homo sapiens (human) | 4249 | MGAT5 |
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| DOID:1793 | pancreatic cancer | HGNC:7047 | Homo sapiens (human) | 11320 | MGAT4A |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:0080433 | developmental and epileptic encephalopathy 51 | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:6000 | congestive heart failure | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:2316 | brain ischemia | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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