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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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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:0090128 | Carvajal syndrome | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0050886 | Troyer syndrome | HGNC:18514 | Homo sapiens (human) | 23111 | SPART |
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| DOID:0112068 | nuclear type mitochondrial complex I deficiency 5 | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:0110142 | Bartter disease type 1 | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
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| DOID:0060861 | microphthalmia with limb anomalies | HGNC:20318 | Homo sapiens (human) | 64093 | SMOC1 |
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| DOID:0110552 | autosomal dominant nonsyndromic deafness 22 | HGNC:7605 | Homo sapiens (human) | 4646 | MYO6 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:18362 | Homo sapiens (human) | 50939 | IMPG2 |
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| DOID:13099 | Moyamoya disease | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:0070048 | GAND syndrome | HGNC:30778 | Homo sapiens (human) | 57459 | GATAD2B |
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| DOID:0110011 | advanced sleep phase syndrome 1 | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
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| DOID:0110629 | Wolfram syndrome 1 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110943 | autosomal recessive osteopetrosis 2 | HGNC:11926 | Homo sapiens (human) | 8600 | TNFSF11 |
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| DOID:0050884 | triosephosphate isomerase deficiency | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0070044 | Coffin-Siris syndrome 2 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0060688 | arteriovenous malformations of the brain | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0060736 | epidermolysis bullosa simplex Ogna type | HGNC:9069 | Homo sapiens (human) | 5339 | PLEC |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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