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GlyTouCan
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:1909 | melanoma | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:9452 | steatotic liver disease | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:11714 | gestational diabetes | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:0080855 | Parkinsonism | HGNC:4244 | Homo sapiens (human) | 2675 | GFRA2 |
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| DOID:0080855 | Parkinsonism | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:2316 | brain ischemia | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:11446 | sciatic neuropathy | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:9810 | polyarteritis nodosa | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4242 | Homo sapiens (human) | 9945 | GFPT2 |
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| DOID:1440 | Machado-Joseph disease | HGNC:4242 | Homo sapiens (human) | 9945 | GFPT2 |
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| DOID:1168 | familial hyperlipidemia | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:9970 | obesity | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:0110660 | congenital myasthenic syndrome 12 | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:1440 | Machado-Joseph disease | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:2018 | hyperinsulinism | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:9268 | glycine encephalopathy | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:9252 | amino acid metabolic disorder | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:557 | kidney disease | HGNC:4201 | Homo sapiens (human) | 2648 | KAT2A |
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