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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:9744 | type 1 diabetes mellitus | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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| DOID:303 | substance-related disorder | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:10283 | prostate cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0080322 | polycystic kidney disease | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0080768 | pyridoxine-dependent epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:2316 | brain ischemia | HGNC:433 | Homo sapiens (human) | 246 | ALOX15 |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0060318 | acute promyelocytic leukemia | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:8778 | Crohn's disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:2152 | ovary epithelial cancer | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:9669 | senile cataract | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8577 | ulcerative colitis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:4450 | renal cell carcinoma | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:224 | transient cerebral ischemia | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0050933 | ovarian serous carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:4897 | bile duct carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:684 | hepatocellular carcinoma | HGNC:24573 | Homo sapiens (human) | 55247 | NEIL3 |
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| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:1612 | breast cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3314 | angiomyolipoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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