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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:9975 | cocaine dependence | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:3669 | intermittent claudication | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:3070 | high grade glioma | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:3963 | thyroid gland carcinoma | HGNC:15855 | Homo sapiens (human) | 22918 | CD93 |
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| DOID:1883 | hepatitis C | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:4231 | histiocytoma | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:11168 | anogenital venereal wart | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:399 | tuberculosis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:12798 | mucopolysaccharidosis | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:9869 | hereditary fructose intolerance syndrome | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:916 | liver benign neoplasm | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:8283 | peritonitis | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0081097 | Rafiq syndrome | MGI:2684954 | Mus musculus (house mouse) | 227619 | Man1b1 |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:5138 | leiomyomatosis | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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