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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:0080337 | mitochondrial DNA depletion syndrome 15 | HGNC:11741 | Homo sapiens (human) | 7019 | TFAM |
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| DOID:0110569 | autosomal dominant nonsyndromic deafness 44 | HGNC:18111 | Homo sapiens (human) | 152137 | CCDC50 |
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| DOID:0050778 | Meckel syndrome | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
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| DOID:8398 | osteoarthritis | HGNC:190 | Homo sapiens (human) | 8038 | ADAM12 |
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| DOID:11981 | morbid obesity | HGNC:15879 | Homo sapiens (human) | 56259 | CTNNBL1 |
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| DOID:3393 | coronary artery disease | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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| DOID:3507 | dermatofibrosarcoma protuberans | HGNC:8800 | Homo sapiens (human) | 5155 | PDGFB |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:10763 | hypertension | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:9975 | cocaine dependence | HGNC:17025 | Homo sapiens (human) | 81578 | COL21A1 |
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| DOID:2626 | choroid plexus papilloma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0060041 | autism spectrum disorder | HGNC:6833 | Homo sapiens (human) | 4128 | MAOA |
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| DOID:10534 | stomach cancer | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:3482 | plague | RGD:620596 | Rattus norvegicus (Norway rat) | 117029 | Ccr5 |
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| DOID:2154 | nephroblastoma | HGNC:9966 | Homo sapiens (human) | 5978 | REST |
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| DOID:2452 | thrombophilia | HGNC:3661 | Homo sapiens (human) | 2243 | FGA |
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| DOID:1612 | breast cancer | HGNC:6585 | Homo sapiens (human) | 3973 | LHCGR |
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| DOID:0070411 | autosomal recessive spinocerebellar ataxia 30 | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:11719 | oculopharyngeal muscular dystrophy | HGNC:8565 | Homo sapiens (human) | 8106 | PABPN1 |
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| DOID:4450 | renal cell carcinoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:4947 | cholangiocarcinoma | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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