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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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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:12801 | mucopolysaccharidosis III | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:10247 | pleurisy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:1580 | diffuse scleroderma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:12361 | Graves' disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080941 | acquired angioedema | HGNC:12823 | Homo sapiens (human) | 7512 | XPNPEP2 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:10534 | stomach cancer | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:971 | tendinitis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:9206 | Barrett's esophagus | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:6196 | reactive arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10591 | pre-eclampsia | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:13619 | extrahepatic cholestasis | HGNC:2605 | Homo sapiens (human) | 1593 | CYP27A1 |
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| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:14330 | Parkinson's disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:2841 | asthma | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:10907 | microcephaly | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:684 | hepatocellular carcinoma | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:684 | hepatocellular carcinoma | HGNC:16066 | Homo sapiens (human) | 55331 | ACER3 |
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| DOID:1596 | depressive disorder | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:2537 | inflammatory and toxic neuropathy | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0050902 | medulloblastoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3526 | cerebral infarction | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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