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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:1793 | pancreatic cancer | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:1612 | breast cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:2752 | glycogen storage disease II | HGNC:4065 | Homo sapiens (human) | 2548 | GAA |
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| DOID:26 | pancreas disease | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:5614 | eye disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:2043 | hepatitis B | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:552 | pneumonia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050700 | cardiomyopathy | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:1024 | leprosy | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:2841 | asthma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:6432 | pulmonary hypertension | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:3534 | Lafora disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:0081168 | HMG-CoA synthase 2 deficiency | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:12217 | Lewy body dementia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:13141 | uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9455 | lipid storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:3454 | brain infarction | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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