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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:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:783 | end stage renal disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:1184 | nephrotic syndrome | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:9743 | diabetic neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:83 | cataract | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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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:9352 | type 2 diabetes mellitus | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:0050700 | cardiomyopathy | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:299 | adenocarcinoma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:9970 | obesity | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:3070 | high grade glioma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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