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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:0112136 | severe congenital neutropenia 4 | MGI:1915651 | Mus musculus (house mouse) | 68401 | G6pc3 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:10534 | stomach cancer | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:1380 | endometrial cancer | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:3069 | malignant astrocytoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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| DOID:0080573 | congenital disorder of glycosylation Ix | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0050453 | lissencephaly | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:10584 | retinitis pigmentosa | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:9884 | muscular dystrophy | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | MGI:1915513 | Mus musculus (house mouse) | 68263 | Pdhb |
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| DOID:2841 | asthma | MGI:1915464 | Mus musculus (house mouse) | 68214 | Gsto2 |
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| DOID:10652 | Alzheimer's disease | MGI:1915464 | Mus musculus (house mouse) | 68214 | Gsto2 |
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| DOID:1574 | alcohol use disorder | MGI:1915464 | Mus musculus (house mouse) | 68214 | Gsto2 |
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| DOID:14330 | Parkinson's disease | MGI:1915464 | Mus musculus (house mouse) | 68214 | Gsto2 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:9970 | obesity | MGI:1915304 | Mus musculus (house mouse) | 68054 | Serpina12 |
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