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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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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:0112080 | nuclear type mitochondrial complex I deficiency 32 | HGNC:7703 | Homo sapiens (human) | 4714 | NDUFB8 |
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| DOID:0081341 | congenital myopathy 5 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:0111625 | ventriculomegaly - cystic kidney disease | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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| DOID:0111950 | immunodeficiency 29 | HGNC:5970 | Homo sapiens (human) | 3593 | IL12B |
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| DOID:2218 | blood platelet disease | HGNC:3393 | Homo sapiens (human) | 2048 | EPHB2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:6188 | Homo sapiens (human) | 182 | JAG1 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0060654 | lethal congenital contracture syndrome 4 | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:0081119 | benign familial infantile seizures 6 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0050975 | spinocerebellar ataxia type 26 | HGNC:3214 | Homo sapiens (human) | 1938 | EEF2 |
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| DOID:0060258 | reticulate acropigmentation of Kitamura | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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| DOID:0112098 | nuclear type mitochondrial complex I deficiency 30 | HGNC:20372 | Homo sapiens (human) | 54539 | NDUFB11 |
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| DOID:9119 | acute myeloid leukemia | HGNC:6679 | Homo sapiens (human) | 4026 | LPP |
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| DOID:0080579 | 3-Methylcrotonyl-CoA carboxylase 1 deficiency | HGNC:6936 | Homo sapiens (human) | 56922 | MCCC1 |
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| DOID:0080136 | multiple mitochondrial dysfunctions syndrome 4 | HGNC:19857 | Homo sapiens (human) | 122961 | ISCA2 |
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| DOID:2394 | ovarian cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:6498 | seborrheic keratosis | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:9269 | maple syrup urine disease | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0111872 | nonphotosensitive trichothiodystrophy 6 | HGNC:4651 | Homo sapiens (human) | 2961 | GTF2E2 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:25777 | Homo sapiens (human) | 64864 | RFX7 |
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| DOID:0050646 | distal arthrogryposis | HGNC:16305 | Homo sapiens (human) | 170689 | ADAMTS15 |
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| DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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