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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3070 | high grade glioma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3146 | lipid metabolism disorder | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:850 | lung disease | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0080750 | erythema nodosum | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:9326 | Homo sapiens (human) | 9374 | PPT2 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:5844 | myocardial infarction | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0060041 | autism spectrum disorder | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:0050771 | pheochromocytoma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:234 | colon adenocarcinoma | HGNC:545 | Homo sapiens (human) | 310 | ANXA7 |
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| DOID:2871 | endometrial carcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:1459 | hypothyroidism | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:9588 | encephalitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:2921 | glomerulonephritis | HGNC:6719 | Homo sapiens (human) | 4056 | LTC4S |
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| DOID:9884 | muscular dystrophy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:1824 | status epilepticus | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:8283 | peritonitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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