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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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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:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2841 | asthma | HGNC:7518 | Homo sapiens (human) | 4589 | MUC7 |
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| DOID:4001 | ovarian carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0111919 | spermatogenic failure 38 | HGNC:23045 | Homo sapiens (human) | 84071 | ARMC2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1508 | Homo sapiens (human) | 840 | CASP7 |
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| DOID:9538 | multiple myeloma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0060898 | Parkinson's disease 20 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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| DOID:0112129 | severe congenital neutropenia 7 | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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| DOID:9884 | muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:20844 | Homo sapiens (human) | 165829 | GPR156 |
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| DOID:9970 | obesity | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:0111322 | idiopathic generalized epilepsy 8 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0050742 | nicotine dependence | HGNC:6528 | Homo sapiens (human) | 3936 | LCP1 |
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| DOID:2349 | arteriosclerosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0070287 | primary autosomal recessive microcephaly 11 | HGNC:3182 | Homo sapiens (human) | 1911 | PHC1 |
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| DOID:1307 | dementia | HGNC:12698 | Homo sapiens (human) | 7436 | VLDLR |
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| DOID:6612 | leukocyte adhesion deficiency | HGNC:6155 | Homo sapiens (human) | 3689 | ITGB2 |
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| DOID:8893 | psoriasis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9351 | diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0050117 | disease by infectious agent | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0060549 | Barber-Say syndrome | HGNC:20670 | Homo sapiens (human) | 117581 | TWIST2 |
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