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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:0112230 | lissencephaly 5 | HGNC:6486 | Homo sapiens (human) | 3912 | LAMB1 |
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| DOID:552 | pneumonia | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0060075 | estrogen-receptor positive breast cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0111904 | autosomal recessive thrombophilia due to protein C deficiency | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:1287 | cardiovascular system disease | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:783 | end stage renal disease | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
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| DOID:10534 | stomach cancer | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:0060797 | hypomyelinating leukodystrophy 8 | HGNC:30348 | Homo sapiens (human) | 55703 | POLR3B |
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| DOID:0090091 | hypogonadotropic hypogonadism 23 with or without anosmia | HGNC:6584 | Homo sapiens (human) | 3972 | LHB |
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| DOID:0080416 | developmental and epileptic encephalopathy 32 | HGNC:6220 | Homo sapiens (human) | 3737 | KCNA2 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:9383 | iridocyclitis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0070471 | early-onset epilepsy 2 | HGNC:29010 | Homo sapiens (human) | 9739 | SETD1A |
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| DOID:0111338 | isolated elevated serum creatine phosphokinase levels | HGNC:27337 | Homo sapiens (human) | 203859 | ANO5 |
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| DOID:4248 | coronary stenosis | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:6014 | Homo sapiens (human) | 3565 | IL4 |
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| DOID:0080188 | chronic myelomonocytic leukemia | HGNC:25941 | Homo sapiens (human) | 54790 | TET2 |
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| DOID:5844 | myocardial infarction | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:0111907 | thrombophilia due to thrombin defect | HGNC:3531 | Homo sapiens (human) | 2162 | F13A1 |
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| DOID:3068 | glioblastoma | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0111669 | hyaline fibromatosis syndrome | HGNC:21732 | Homo sapiens (human) | 118429 | ANTXR2 |
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| DOID:0080264 | exudative vitreoretinopathy 7 | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:18533 | Homo sapiens (human) | 84196 | USP48 |
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| DOID:9261 | nasopharynx carcinoma | HGNC:6844 | Homo sapiens (human) | 6416 | MAP2K4 |
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