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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:0080046 | Stickler syndrome | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0070474 | childhood-onset neurodegeneration with brain atrophy | HGNC:12511 | Homo sapiens (human) | 7343 | UBTF |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0110573 | autosomal dominant nonsyndromic deafness 4A | HGNC:23212 | Homo sapiens (human) | 79784 | MYH14 |
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| DOID:0081125 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 | HGNC:15870 | Homo sapiens (human) | 55969 | RAB5IF |
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| DOID:0060428 | SATB2-associated syndrome | HGNC:21637 | Homo sapiens (human) | 23314 | SATB2 |
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| DOID:4549 | extraskeletal myxoid chondrosarcoma | HGNC:7982 | Homo sapiens (human) | 8013 | NR4A3 |
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| DOID:0111948 | immunodeficiency 46 | HGNC:11763 | Homo sapiens (human) | 7037 | TFRC |
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| DOID:2394 | ovarian cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:237 | Homo sapiens (human) | 112 | ADCY6 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:19070 | Homo sapiens (human) | 9984 | THOC1 |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:10993 | Homo sapiens (human) | 10861 | SLC26A1 |
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| DOID:13099 | Moyamoya disease | HGNC:21625 | Homo sapiens (human) | 55107 | ANO1 |
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| DOID:0081001 | Cowden syndrome 5 | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:4423 | sea-blue histiocytosis | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0070053 | autosomal dominant intellectual developmental disorder 23 | HGNC:25566 | Homo sapiens (human) | 55209 | SETD5 |
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| DOID:3144 | cutis laxa | HGNC:3218 | Homo sapiens (human) | 2202 | EFEMP1 |
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| DOID:0081359 | epidermolytic hyperkeratosis 2 | HGNC:6413 | Homo sapiens (human) | 3858 | KRT10 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0110732 | neuronal ceroid lipofuscinosis 11 | HGNC:4601 | Homo sapiens (human) | 2896 | GRN |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:0111952 | immunodeficiency 57 | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:0070483 | Watson syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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