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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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| DOID:409 | liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:3310 | atopic dermatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0080199 | colorectal carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0081002 | Cowden syndrome 6 | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:9974 | drug dependence | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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| DOID:2841 | asthma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:13189 | gout | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:783 | end stage renal disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:2841 | asthma | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0060673 | Peters anomaly | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:1287 | cardiovascular system disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10652 | Alzheimer's disease | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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