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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: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:0050820 | atrioventricular block | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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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:1558 | angioedema | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:0080199 | colorectal carcinoma | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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| DOID:0112354 | spermatogenic failure 65 | HGNC:26532 | Homo sapiens (human) | 144132 | DNHD1 |
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| DOID:2377 | multiple sclerosis | HGNC:4951 | Homo sapiens (human) | 3125 | HLA-DRB3 |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:8466 | retinal degeneration | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:76 | stomach disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0070383 | developmental and epileptic encephalopathy 97 | HGNC:2550 | Homo sapiens (human) | 10659 | CELF2 |
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| DOID:0080828 | VEXAS syndrome | HGNC:12469 | Homo sapiens (human) | 7317 | UBA1 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:12365 | malaria | HGNC:4704 | Homo sapiens (human) | 2995 | GYPC |
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| DOID:3393 | coronary artery disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0050887 | Townes-Brocks syndrome | HGNC:17748 | Homo sapiens (human) | 51339 | DACT1 |
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| DOID:0111275 | speech-language disorder-1 | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:8947 | diabetic retinopathy | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:14040 | autoimmune polyendocrine syndrome | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080797 | nasal type extranodal NK/T-cell lymphoma | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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