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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:0111941 | immunodeficiency 20 | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9834 | hyperopia | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1967 | leiomyosarcoma | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:9974 | drug dependence | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:783 | end stage renal disease | HGNC:338 | Homo sapiens (human) | 186 | AGTR2 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:399 | tuberculosis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:3312 | bipolar disorder | HGNC:701 | Homo sapiens (human) | 406 | BMAL1 |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:14040 | autoimmune polyendocrine syndrome | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111162 | epidermal nevus | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:1825 | childhood absence epilepsy | HGNC:18712 | Homo sapiens (human) | 163175 | LGI4 |
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| DOID:12858 | Huntington's disease | HGNC:4585 | Homo sapiens (human) | 2903 | GRIN2A |
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| DOID:0111699 | Van den Ende-Gupta syndrome | HGNC:19869 | Homo sapiens (human) | 91179 | SCARF2 |
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| DOID:2366 | West Nile fever | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0050741 | alcohol dependence | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:8923 | skin melanoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:11044 | gastroschisis | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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