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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:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:8778 | Crohn's disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2018 | hyperinsulinism | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:1168 | familial hyperlipidemia | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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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 | HGNC:12540 | Homo sapiens (human) | 54576 | UGT1A8 |
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| DOID:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1380 | endometrial cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:670 | amphetamine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:13580 | cholestasis | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:1591 | renovascular hypertension | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:363 | uterine cancer | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:1459 | hypothyroidism | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:219 | colon cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3571 | liver cancer | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:1485 | cystic fibrosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10534 | stomach cancer | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:11446 | sciatic neuropathy | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1287 | cardiovascular system disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:4194 | glucose metabolism disease | HGNC:2849 | Homo sapiens (human) | 1606 | DGKA |
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