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GlyTouCan
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:9970 | obesity | MGI:1202879 | Mus musculus (house mouse) | 21416 | Tcf7l2 |
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| DOID:9256 | colorectal cancer | MGI:1202879 | Mus musculus (house mouse) | 21416 | Tcf7l2 |
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| DOID:1612 | breast cancer | MGI:1202879 | Mus musculus (house mouse) | 21416 | Tcf7l2 |
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| DOID:11714 | gestational diabetes | MGI:1202879 | Mus musculus (house mouse) | 21416 | Tcf7l2 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3518 | Homo sapiens (human) | 2137 | EXTL3 |
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| DOID:2978 | carbohydrate metabolic disorder | MGI:1274789 | Mus musculus (house mouse) | 21351 | Taldo1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3515 | Homo sapiens (human) | 2134 | EXTL1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3513 | Homo sapiens (human) | 2132 | EXT2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:3371 | chondrosarcoma | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | MGI:2384851 | Mus musculus (house mouse) | 213053 | Slc39a14 |
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| DOID:4194 | glucose metabolism disease | MGI:2670962 | Mus musculus (house mouse) | 212032 | Hk3 |
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| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | MGI:2442253 | Mus musculus (house mouse) | 211286 | Cln5 |
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| DOID:676 | juvenile rheumatoid arthritis | MGI:2445077 | Mus musculus (house mouse) | 210808 | Lacc1 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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| DOID:5212 | congenital disorder of glycosylation | MGI:1098592 | Mus musculus (house mouse) | 208624 | Alg3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | MGI:1098592 | Mus musculus (house mouse) | 208624 | Alg3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:5212 | congenital disorder of glycosylation | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:326 | ischemia | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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