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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:14566 | disease of cellular proliferation | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:9970 | obesity | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:9655 | oral mucosa leukoplakia | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:9120 | amyloidosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
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| DOID:2237 | hepatitis | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:14717 | centronuclear myopathy | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
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| DOID:4247 | coronary restenosis | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:12236 | primary biliary cholangitis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:11714 | gestational diabetes | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:1824 | status epilepticus | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0112361 | spondylocostal dysostosis 3 | HGNC:6560 | Homo sapiens (human) | 3955 | LFNG |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
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| DOID:1287 | cardiovascular system disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:11714 | gestational diabetes | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:14115 | toxic shock syndrome | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080582 | hypotrichosis 14 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:162 | cancer | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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