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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:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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| DOID:9975 | cocaine dependence | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:3669 | intermittent claudication | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:3070 | high grade glioma | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:3070 | high grade glioma | HGNC:10860 | Homo sapiens (human) | 6480 | ST6GAL1 |
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| DOID:1574 | alcohol use disorder | HGNC:10860 | Homo sapiens (human) | 6480 | ST6GAL1 |
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| DOID:0060180 | colitis | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:162 | cancer | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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| DOID:5419 | schizophrenia | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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| DOID:1574 | alcohol use disorder | HGNC:10852 | Homo sapiens (human) | 6472 | SHMT2 |
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| DOID:162 | cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:2394 | ovarian cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:1574 | alcohol use disorder | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:1612 | breast cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:0111395 | mucopolysaccharidosis type IIIA | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:1184 | nephrotic syndrome | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:9970 | obesity | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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