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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:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:12732 | intermediate uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10591 | pre-eclampsia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:417 | autoimmune disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10763 | hypertension | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:12129 | bulimia nervosa | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:4249 | Gerstmann-Straussler-Scheinker syndrome | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:4079 | heart valve disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:12798 | mucopolysaccharidosis | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:10283 | prostate cancer | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10652 | Alzheimer's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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