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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
LM-GlycoRepo
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:4607 | biliary tract cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:2355 | anemia | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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| DOID:0090124 | neurogenic-type arthrogryposis multiplex congenita-2 | HGNC:29205 | Homo sapiens (human) | 57222 | ERGIC1 |
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| DOID:0111957 | immunodeficiency 11A | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:12306 | vitiligo | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0060496 | respiratory allergy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:3765 | Homo sapiens (human) | 2322 | FLT3 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0081228 | autosomal recessive intellectual developmental disorder 67 | HGNC:3275 | Homo sapiens (human) | 8665 | EIF3F |
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| DOID:0060884 | renal hypomagnesemia 6 | HGNC:103 | Homo sapiens (human) | 54805 | CNNM2 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:3010 | Homo sapiens (human) | 1804 | DPP6 |
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| DOID:8929 | atrophic gastritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:10322 | berylliosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:5419 | schizophrenia | HGNC:922 | Homo sapiens (human) | 135152 | B3GAT2 |
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| DOID:0080600 | COVID-19 | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:11054 | urinary bladder cancer | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:1474 | aggressive periodontitis | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:0050523 | adult T-cell leukemia/lymphoma | HGNC:7881 | Homo sapiens (human) | 4851 | NOTCH1 |
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| DOID:2596 | larynx cancer | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:2377 | multiple sclerosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:0111351 | D-2-hydroxyglutaric aciduria 1 | HGNC:28358 | Homo sapiens (human) | 728294 | D2HGDH |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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