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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:1612 | breast cancer | HGNC:5012 | Homo sapiens (human) | 3161 | HMMR |
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| DOID:2977 | primary hyperoxaluria | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:0112127 | HRPT-related hyperuricemia | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:0050816 | urofacial syndrome | HGNC:18374 | Homo sapiens (human) | 60495 | HPSE2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:219 | colon cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:1793 | pancreatic cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:1324 | lung cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:9970 | obesity | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0090140 | cortisone reductase deficiency 2 | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10825 | essential hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:3393 | coronary artery disease | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10763 | hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:1824 | status epilepticus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10591 | pre-eclampsia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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