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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:9870 | galactosemia | SGD:S000000223 | Saccharomyces cerevisiae S288C | 852307 | GAL10 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | SGD:S000005185 | Saccharomyces cerevisiae S288C | 855480 | ZWF1 |
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| DOID:2750 | glycogen storage disease IV | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9291 | Homo sapiens (human) | 5506 | PPP1R3A |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2841 | asthma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:3803 | Crigler-Najjar syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9970 | obesity | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:10763 | hypertension | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:83 | cataract | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:1926 | Gaucher's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0111077 | pyruvate kinase deficiency of red cells | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:12894 | Sjogren's syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:3347 | osteosarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10763 | hypertension | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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