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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:2747 | glycogen storage disease | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:3138 | acanthosis nigricans | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:10763 | hypertension | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:10652 | Alzheimer's disease | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:9351 | diabetes mellitus | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:83 | cataract | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:6000 | congestive heart failure | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:3393 | coronary artery disease | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:6432 | pulmonary hypertension | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:104 | bacterial infectious disease | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0050775 | schneckenbecken dysplasia | HGNC:20800 | Homo sapiens (human) | 23169 | SLC35D1 |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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| DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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