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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9119 | acute myeloid leukemia | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:1561 | cognitive disorder | HGNC:610 | Homo sapiens (human) | 345 | APOC3 |
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| DOID:0081137 | agammaglobulinemia 3 | HGNC:1698 | Homo sapiens (human) | 973 | CD79A |
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| DOID:12306 | vitiligo | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0111901 | heparin cofactor II deficiency | HGNC:4838 | Homo sapiens (human) | 3053 | SERPIND1 |
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| DOID:14330 | Parkinson's disease | HGNC:30343 | Homo sapiens (human) | 23317 | DNAJC13 |
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| DOID:0110574 | autosomal dominant nonsyndromic deafness 4B | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:13241 | Behcet's disease | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:12297 | Vogt-Koyanagi-Harada disease | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:399 | tuberculosis | HGNC:5439 | Homo sapiens (human) | 3459 | IFNGR1 |
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| DOID:2508 | Takayasu's arteritis | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:0111314 | idiopathic generalized epilepsy 13 | HGNC:4075 | Homo sapiens (human) | 2554 | GABRA1 |
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| DOID:1882 | atrial heart septal defect | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:8869 | neuromyelitis optica | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050567 | orofacial cleft | HGNC:26521 | Homo sapiens (human) | 125336 | LOXHD1 |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:9256 | colorectal cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:12271 | aniridia | HGNC:1171 | Homo sapiens (human) | 26610 | ELP4 |
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| DOID:3407 | carotid artery disease | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:6419 | tetralogy of Fallot | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:1324 | lung cancer | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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