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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:6713 | cerebrovascular disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4195 | hyperglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:1612 | breast cancer | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:10300 | Raynaud disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10273 | heart conduction disease | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:5082 | liver cirrhosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:10763 | hypertension | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
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| DOID:9452 | steatotic liver disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:1936 | atherosclerosis | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:1574 | alcohol use disorder | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:10140 | dry eye syndrome | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:13641 | exfoliation syndrome | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:3343 | glycoproteinosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
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| DOID:14681 | Silver-Russell syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:9976 | heroin dependence | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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