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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
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:0081339 | congenital myopathy 2B | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:12886 | Homo sapiens (human) | 64397 | ZNF106 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:12869 | Homo sapiens (human) | 7543 | ZFX |
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| DOID:627 | severe combined immunodeficiency | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:0111943 | immunodeficiency 48 | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:7148 | rheumatoid arthritis | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12856 | Homo sapiens (human) | 7528 | YY1 |
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| DOID:4769 | pleuropulmonary blastoma | HGNC:12856 | Homo sapiens (human) | 7528 | YY1 |
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| DOID:6000 | congestive heart failure | HGNC:12856 | Homo sapiens (human) | 7528 | YY1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:1059 | intellectual disability | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:11832 | visual epilepsy | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:5419 | schizophrenia | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:1825 | childhood absence epilepsy | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:10763 | hypertension | HGNC:12855 | Homo sapiens (human) | 7534 | YWHAZ |
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| DOID:1059 | intellectual disability | HGNC:12854 | Homo sapiens (human) | 10971 | YWHAQ |
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| DOID:0080282 | developmental and epileptic encephalopathy 56 | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:0060480 | left ventricular noncompaction | HGNC:12851 | Homo sapiens (human) | 7531 | YWHAE |
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| DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:12851 | Homo sapiens (human) | 7531 | YWHAE |
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| DOID:700 | mitochondrial metabolism disease | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
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| DOID:0111436 | optic atrophy 11 | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:12840 | Homo sapiens (human) | 8565 | YARS1 |
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