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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:0110168 | Charcot-Marie-Tooth disease type 2Y | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0070097 | oculocutaneous albinism type III | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:3565 | meningioma | HGNC:11109 | Homo sapiens (human) | 6605 | SMARCE1 |
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| DOID:1389 | polyneuropathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:4448 | macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10446 | Homo sapiens (human) | 6236 | RRAD |
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| DOID:0070389 | developmental and epileptic encephalopathy 103 | HGNC:6234 | Homo sapiens (human) | 3747 | KCNC2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:8893 | psoriasis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:9970 | obesity | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:14330 | Parkinson's disease | HGNC:4947 | Homo sapiens (human) | 3122 | HLA-DRA |
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| DOID:0080445 | developmental and epileptic encephalopathy 13 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:12894 | Sjogren's syndrome | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:0090083 | hypogonadotropic hypogonadism 2 with or without anosmia | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:0110025 | age related macular degeneration 13 | HGNC:5394 | Homo sapiens (human) | 3426 | CFI |
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| DOID:6432 | pulmonary hypertension | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:11212 | hydrophthalmos | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:1612 | breast cancer | HGNC:9646 | Homo sapiens (human) | 5783 | PTPN13 |
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| DOID:0111864 | autosomal recessive congenital bilateral absence of vas deferens | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:10646 | schizotypal personality disorder | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
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| DOID:0060041 | autism spectrum disorder | HGNC:29849 | Homo sapiens (human) | 253559 | CADM2 |
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