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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
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:0111816 | syndactyly type 1 | HGNC:5956 | Homo sapiens (human) | 3549 | IHH |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1959 | Homo sapiens (human) | 1138 | CHRNA5 |
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| DOID:612 | primary immunodeficiency disease | HGNC:7562 | Homo sapiens (human) | 4615 | MYD88 |
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| DOID:1380 | endometrial cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:0111347 | epidermolysis bullosa with congenital localized absence of skin and deformity of nails | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:8499 | night blindness | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:3393 | coronary artery disease | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080162 | lupus nephritis | HGNC:6371 | Homo sapiens (human) | 3818 | KLKB1 |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:252 | alcoholic psychosis | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:12714 | Ellis-Van Creveld syndrome | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:5082 | liver cirrhosis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:850 | lung disease | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:8398 | osteoarthritis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:841 | extrinsic allergic alveolitis | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:0081340 | congenital myopathy 2C | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081163 | dilated cardiomyopathy 2G | HGNC:6648 | Homo sapiens (human) | 442721 | LMOD2 |
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| DOID:5844 | myocardial infarction | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0110969 | brachydactyly type B1 | HGNC:10257 | Homo sapiens (human) | 4920 | ROR2 |
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| DOID:11119 | Gilles de la Tourette syndrome | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:11981 | morbid obesity | HGNC:6932 | Homo sapiens (human) | 4160 | MC4R |
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