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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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MIRAGE
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:1596 | depressive disorder | HGNC:8154 | Homo sapiens (human) | 4986 | OPRK1 |
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| DOID:746 | adenomatoid tumor | HGNC:20456 | Homo sapiens (human) | 84231 | TRAF7 |
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| DOID:0060708 | lymphoproliferative syndrome 2 | HGNC:11922 | Homo sapiens (human) | 939 | CD27 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:4947 | Homo sapiens (human) | 3122 | HLA-DRA |
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| DOID:0060788 | hypomyelinating leukodystrophy 10 | HGNC:30262 | Homo sapiens (human) | 29920 | PYCR2 |
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| DOID:0080420 | developmental and epileptic encephalopathy 62 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0111786 | frontometaphyseal dysplasia 1 | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:1588 | thrombocytopenia | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0110054 | amelogenesis imperfecta type 1A | HGNC:6490 | Homo sapiens (human) | 3914 | LAMB3 |
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| DOID:418 | systemic scleroderma | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0112314 | brain small vessel disease 2 | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:2394 | ovarian cancer | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:0110815 | hereditary spastic paraplegia 64 | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:1059 | intellectual disability | HGNC:685 | Homo sapiens (human) | 9459 | ARHGEF6 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0110200 | Charcot-Marie-Tooth disease dominant intermediate D | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:6029 | Homo sapiens (human) | 3578 | IL9 |
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| DOID:8398 | osteoarthritis | HGNC:1980 | Homo sapiens (human) | 8483 | CILP |
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| DOID:12930 | dilated cardiomyopathy | HGNC:16932 | Homo sapiens (human) | 10529 | NEBL |
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| DOID:0110247 | cataract 36 | HGNC:30831 | Homo sapiens (human) | 23424 | TDRD7 |
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| DOID:10534 | stomach cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:11476 | osteoporosis | HGNC:1440 | Homo sapiens (human) | 799 | CALCR |
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| DOID:9206 | Barrett's esophagus | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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