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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
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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:12851 | Homo sapiens (human) | 7531 | YWHAE |
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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: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: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:326 | ischemia | HGNC:12950 | Homo sapiens (human) | 7536 | SF1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:1922637 | Mus musculus (house mouse) | 75387 | Sirt4 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:684 | hepatocellular carcinoma | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:1612 | breast cancer | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:1682 | congenital heart disease | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:0050861 | colorectal adenocarcinoma | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:0060936 | dystonia 28 childhood-onset | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:10283 | prostate cancer | MGI:109565 | Mus musculus (house mouse) | 75410 | Kmt2b |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:12869 | Homo sapiens (human) | 7543 | ZFX |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | MGI:1919824 | Mus musculus (house mouse) | 75553 | Zc3h14 |
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| DOID:0081217 | autosomal recessive intellectual developmental disorder 56 | MGI:1919824 | Mus musculus (house mouse) | 75553 | Zc3h14 |
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| DOID:1059 | intellectual disability | MGI:1919824 | Mus musculus (house mouse) | 75553 | Zc3h14 |
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