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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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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:0111541 | pigmented paravenous chorioretinal atrophy | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:2747 | glycogen storage disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2043 | hepatitis B | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:9976 | heroin dependence | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:557 | kidney disease | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
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| DOID:2043 | hepatitis B | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9970 | obesity | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:14764 | Larsen syndrome | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:1682 | congenital heart disease | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:3261 | hyper IgE recurrent infection syndrome 1 | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:674 | cleft palate | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:9538 | multiple myeloma | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:1580 | diffuse scleroderma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:13916 | Homo sapiens (human) | 55937 | APOM |
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| DOID:0111667 | enterokinase deficiency | HGNC:9490 | Homo sapiens (human) | 5651 | TMPRSS15 |
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| DOID:10003 | sensorineural hearing loss | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:12361 | Graves' disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:1793 | pancreatic cancer | HGNC:882 | Homo sapiens (human) | 545 | ATR |
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| DOID:0111618 | autosomal recessive spinocerebellar ataxia 8 | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:10763 | hypertension | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:9970 | obesity | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:11726 | Emery-Dreifuss muscular dystrophy | HGNC:3331 | Homo sapiens (human) | 2010 | EMD |
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