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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1070 | primary open angle glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:0110373 | retinitis pigmentosa 61 | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:5844 | myocardial infarction | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:9258 | Waardenburg syndrome | HGNC:7105 | Homo sapiens (human) | 4286 | MITF |
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| DOID:783 | end stage renal disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111131 | focal segmental glomerulosclerosis 6 | HGNC:7599 | Homo sapiens (human) | 4643 | MYO1E |
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| DOID:11476 | osteoporosis | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0050902 | medulloblastoma | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:0112158 | De Sanctis-Cacchione syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3595 | Homo sapiens (human) | 2195 | FAT1 |
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| DOID:0050784 | primary progressive multiple sclerosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0111469 | combined oxidative phosphorylation deficiency 16 | HGNC:16650 | Homo sapiens (human) | 65080 | MRPL44 |
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| DOID:0111974 | immunodeficiency 59 | HGNC:16931 | Homo sapiens (human) | 10525 | HYOU1 |
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| DOID:0111418 | familial apolipoprotein C-II deficiency | HGNC:609 | Homo sapiens (human) | 344 | APOC2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:5844 | myocardial infarction | HGNC:9535 | Homo sapiens (human) | 5687 | PSMA6 |
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| DOID:0110823 | hereditary spastic paraplegia 8 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:5409 | lung small cell carcinoma | HGNC:3595 | Homo sapiens (human) | 2195 | FAT1 |
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| DOID:178 | vascular disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:0110727 | neuronal ceroid lipofuscinosis 13 | HGNC:2531 | Homo sapiens (human) | 8722 | CTSF |
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| DOID:12241 | beta thalassemia | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:1387 | hypolipoproteinemia | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
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