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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:3068 | glioblastoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1612 | breast cancer | HGNC:2637 | Homo sapiens (human) | 1576 | CYP3A4 |
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| DOID:8955 | sideroblastic anemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:1184 | nephrotic syndrome | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:670 | amphetamine abuse | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:13608 | biliary atresia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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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:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:988 | mitral valve prolapse | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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