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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:0112040 | non-syndromic X-linked intellectual disability 100 | HGNC:13339 | Homo sapiens (human) | 24137 | KIF4A |
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| DOID:0090070 | hypogonadotropic hypogonadism | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
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| DOID:0050858 | Marshall-Smith syndrome | HGNC:7788 | Homo sapiens (human) | 4784 | NFIX |
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| DOID:0040091 | autoimmune pancreatitis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0111577 | dehydrated hereditary stomatocytosis 2 | HGNC:6293 | Homo sapiens (human) | 3783 | KCNN4 |
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| DOID:3450 | cutaneous Paget's disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0080727 | Ehlers-Danlos syndrome arthrochalasia type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:5844 | myocardial infarction | HGNC:6357 | Homo sapiens (human) | 3816 | KLK1 |
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| DOID:1395 | schistosomiasis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0080807 | autosomal dominant craniodiaphyseal dysplasia | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
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| DOID:2893 | cervix carcinoma | HGNC:18173 | Homo sapiens (human) | 51752 | ERAP1 |
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| DOID:5844 | myocardial infarction | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:2531 | hematologic cancer | HGNC:10937 | Homo sapiens (human) | 6573 | SLC19A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:9707 | Homo sapiens (human) | 5819 | NECTIN2 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:13378 | Kawasaki disease | HGNC:5234 | Homo sapiens (human) | 3305 | HSPA1L |
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| DOID:114 | heart disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0070120 | Meckel syndrome 6 | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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| DOID:10763 | hypertension | RGD:620349 | Rattus norvegicus (Norway rat) | 29527 | Ptgs2 |
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| DOID:2218 | blood platelet disease | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:1474 | aggressive periodontitis | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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