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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:0050567 | orofacial cleft | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:1574 | alcohol use disorder | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:11981 | morbid obesity | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:2841 | asthma | HGNC:15634 | Homo sapiens (human) | 81793 | TLR10 |
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| DOID:557 | kidney disease | HGNC:15583 | Homo sapiens (human) | 197021 | LCTL |
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| DOID:557 | kidney disease | HGNC:15527 | Homo sapiens (human) | 152831 | KLB |
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| DOID:0080322 | polycystic kidney disease | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:557 | kidney disease | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:10908 | hydrocephalus | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:784 | chronic kidney disease | HGNC:1548 | Homo sapiens (human) | 873 | CBR1 |
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| DOID:10273 | heart conduction disease | HGNC:15460 | Homo sapiens (human) | 55799 | CACNA2D3 |
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| DOID:1459 | hypothyroidism | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10825 | essential hypertension | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:161 | keratosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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