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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:0080579 | 3-Methylcrotonyl-CoA carboxylase 1 deficiency | MGI:1919289 | Mus musculus (house mouse) | 72039 | Mccc1 |
|
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:1826 | epilepsy | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
|
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| DOID:0050908 | myelodysplastic syndrome | MGI:1919297 | Mus musculus (house mouse) | 72047 | Ddx42 |
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| DOID:0081147 | common variable immunodeficiency 4 | MGI:1919299 | Mus musculus (house mouse) | 72049 | Tnfrsf13c |
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| DOID:1574 | alcohol use disorder | MGI:1919307 | Mus musculus (house mouse) | 72057 | Phf10 |
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| DOID:1925 | Coffin-Siris syndrome | MGI:1919307 | Mus musculus (house mouse) | 72057 | Phf10 |
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| DOID:12361 | Graves' disease | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:0060298 | complement component 4b deficiency | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:12849 | autistic disorder | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:4450 | renal cell carcinoma | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:7148 | rheumatoid arthritis | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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||
| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | MGI:1919386 | Mus musculus (house mouse) | 72136 | Chst14 |
|
||
| DOID:2935 | Chediak-Higashi syndrome | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:0060041 | autism spectrum disorder | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:0070295 | primary autosomal dominant microcephaly 18 | MGI:1096875 | Mus musculus (house mouse) | 72145 | Wdfy3 |
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| DOID:3307 | teratoma | MGI:97565 | Mus musculus (house mouse) | 72157 | Pgm1 |
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| DOID:1380 | endometrial cancer | MGI:97565 | Mus musculus (house mouse) | 72157 | Pgm1 |
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| DOID:0080570 | congenital disorder of glycosylation It | MGI:97565 | Mus musculus (house mouse) | 72157 | Pgm1 |
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| DOID:1508 | candidiasis | MGI:1919412 | Mus musculus (house mouse) | 72162 | Dhx36 |
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| DOID:0110722 | neuronal ceroid lipofuscinosis 7 | MGI:1919425 | Mus musculus (house mouse) | 72175 | Mfsd8 |
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| DOID:0080600 | COVID-19 | HGNC:1325 | Homo sapiens (human) | 722 | C4BPA |
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| DOID:6432 | pulmonary hypertension | HGNC:12335 | Homo sapiens (human) | 7222 | TRPC3 |
|
