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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:12689 | acoustic neuroma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:12802 | mucopolysaccharidosis I | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:12858 | Huntington's disease | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18431 | Homo sapiens (human) | 10965 | ACOT2 |
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| DOID:9538 | multiple myeloma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:14227 | azoospermia | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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| DOID:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:12577 | urethral obstruction | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:4989 | pancreatitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:12700 | hyperprolactinemia | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:10241 | thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11996 | spermatic cord torsion | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:2377 | multiple sclerosis | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:10763 | hypertension | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:10763 | hypertension | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:5419 | schizophrenia | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:9408 | acute myocardial infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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