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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:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0081319 | multiple synostoses syndrome 3 | HGNC:3687 | Homo sapiens (human) | 2254 | FGF9 |
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| DOID:0111346 | epidermolysis bullosa simplex with mottled pigmentation | HGNC:6442 | Homo sapiens (human) | 3852 | KRT5 |
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| DOID:2154 | nephroblastoma | HGNC:9966 | Homo sapiens (human) | 5978 | REST |
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| DOID:0081109 | keratosis palmoplantaris striata 2 | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0080860 | primary ovarian insufficiency 3 | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:0110856 | posterior polymorphous corneal dystrophy 2 | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
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| DOID:0080074 | neural tube defect | HGNC:26219 | Homo sapiens (human) | 80199 | FUZ |
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| DOID:0080959 | arrhythmogenic right ventricular dysplasia 14 | HGNC:1759 | Homo sapiens (human) | 1000 | CDH2 |
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| DOID:0111699 | Van den Ende-Gupta syndrome | HGNC:19869 | Homo sapiens (human) | 91179 | SCARF2 |
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| DOID:0080329 | cold-induced sweating syndrome 1 | HGNC:2364 | Homo sapiens (human) | 9244 | CRLF1 |
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| DOID:0050942 | spastic ataxia 3 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:0110536 | autosomal recessive nonsyndromic deafness 91 | HGNC:8950 | Homo sapiens (human) | 5269 | SERPINB6 |
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| DOID:0080545 | hyper IgE syndrome | HGNC:6019 | Homo sapiens (human) | 3570 | IL6R |
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| DOID:0080940 | hereditary angioedema type III | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:0081343 | congenital myopathy 9A | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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| DOID:0112064 | immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis | HGNC:9802 | Homo sapiens (human) | 5880 | RAC2 |
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| DOID:12558 | chronic progressive external ophthalmoplegia | HGNC:10451 | Homo sapiens (human) | 6240 | RRM1 |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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| DOID:0112193 | tetraamelia syndrome 2 | HGNC:28583 | Homo sapiens (human) | 340419 | RSPO2 |
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| DOID:0112354 | spermatogenic failure 65 | HGNC:26532 | Homo sapiens (human) | 144132 | DNHD1 |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0070383 | developmental and epileptic encephalopathy 97 | HGNC:2550 | Homo sapiens (human) | 10659 | CELF2 |
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