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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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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:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:397 | restrictive cardiomyopathy | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:305 | carcinoma | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:2018 | hyperinsulinism | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:2581 | chondrodysplasia punctata | HGNC:10545 | Homo sapiens (human) | 6307 | MSMO1 |
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| DOID:10825 | essential hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:10763 | hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:9282 | ocular hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:8577 | ulcerative colitis | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:0110530 | autosomal recessive nonsyndromic deafness 84B | MGI:3647600 | Mus musculus (house mouse) | 628870 | Otogl |
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| DOID:7998 | hyperthyroidism | HGNC:1027 | Homo sapiens (human) | 622 | BDH1 |
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| DOID:0080600 | COVID-19 | HGNC:1027 | Homo sapiens (human) | 622 | BDH1 |
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| DOID:4947 | cholangiocarcinoma | MGI:3576090 | Mus musculus (house mouse) | 613123 | Ugt1a8 |
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| DOID:4988 | alcoholic pancreatitis | MGI:3576090 | Mus musculus (house mouse) | 613123 | Ugt1a8 |
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| DOID:1793 | pancreatic cancer | MGI:3576090 | Mus musculus (house mouse) | 613123 | Ugt1a8 |
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| DOID:1508 | candidiasis | RGD:619954 | Rattus norvegicus (Norway rat) | 60670 | Fut4 |
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| DOID:0080855 | Parkinsonism | MGI:2152453 | Mus musculus (house mouse) | 606496 | Gsk3a |
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| DOID:332 | amyotrophic lateral sclerosis | MGI:2152453 | Mus musculus (house mouse) | 606496 | Gsk3a |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:8499 | night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050534 | congenital stationary night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050816 | urofacial syndrome | HGNC:18374 | Homo sapiens (human) | 60495 | HPSE2 |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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