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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:1324 | lung cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:10591 | pre-eclampsia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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| DOID:1485 | cystic fibrosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:0080633 | developmental cardiac valvular defect | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:9256 | colorectal cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:2571 | Langerhans-cell histiocytosis | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:820 | myocarditis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:326 | ischemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:11476 | osteoporosis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:0050453 | lissencephaly | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:678 | progressive supranuclear palsy | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:10159 | osteonecrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:684 | hepatocellular carcinoma | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:3328 | temporal lobe epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:2841 | asthma | HGNC:15634 | Homo sapiens (human) | 81793 | TLR10 |
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| DOID:3393 | coronary artery disease | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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| DOID:423 | myopathy | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:399 | tuberculosis | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0060786 | hypomyelinating leukodystrophy | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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