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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:0070046 | Coffin-Siris syndrome 4 | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:0080750 | erythema nodosum | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12732 | intermediate uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080758 | Fanconi renotubular syndrome 2 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0111990 | immunodeficiency 30 | HGNC:5971 | Homo sapiens (human) | 3594 | IL12RB1 |
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| DOID:418 | systemic scleroderma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:399 | tuberculosis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:14450 | 46 XX gonadal dysgenesis | HGNC:3969 | Homo sapiens (human) | 2492 | FSHR |
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| DOID:8923 | skin melanoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:12849 | autistic disorder | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:7728 | Homo sapiens (human) | 23327 | NEDD4L |
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| DOID:1380 | endometrial cancer | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:2841 | asthma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:0110463 | autosomal recessive nonsyndromic deafness 102 | HGNC:3420 | Homo sapiens (human) | 2059 | EPS8 |
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| DOID:0081061 | nephrogenic diabetes insipidus type 2 | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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| DOID:3393 | coronary artery disease | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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| DOID:3526 | cerebral infarction | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:0080077 | hypophosphatemic nephrolithiasis/osteoporosis 1 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:6000 | congestive heart failure | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:0050777 | Joubert syndrome | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:2377 | multiple sclerosis | HGNC:6925 | Homo sapiens (human) | 4155 | MBP |
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| DOID:0111863 | X-linked congenital bilateral absence of vas deferens | HGNC:4516 | Homo sapiens (human) | 10149 | ADGRG2 |
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| DOID:0060916 | proteasome-associated autoinflammatory syndrome 3 | HGNC:9541 | Homo sapiens (human) | 5692 | PSMB4 |
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