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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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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:576 | proteinuria | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0080634 | nanophthalmos | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
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| DOID:2256 | osteochondrodysplasia | HGNC:6909 | Homo sapiens (human) | 4148 | MATN3 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:633 | myositis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:5419 | schizophrenia | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0060001 | withdrawal disorder | HGNC:17071 | Homo sapiens (human) | 23081 | KDM4C |
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| DOID:13258 | typhoid fever | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:9351 | diabetes mellitus | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
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| DOID:5419 | schizophrenia | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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| DOID:8398 | osteoarthritis | HGNC:1980 | Homo sapiens (human) | 8483 | CILP |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:11335 | sarcoidosis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0050648 | atelosteogenesis | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0110220 | Brugada syndrome 3 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0112373 | autosomal dominant auditory neuropathy 3 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
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| DOID:13258 | typhoid fever | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:13336 | congenital toxoplasmosis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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