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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:3892 | insulinoma | RGD:2915 | Rattus norvegicus (Norway rat) | 24505 | Ins1 |
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| DOID:162 | cancer | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:612 | primary immunodeficiency disease | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:1308903 | Rattus norvegicus (Norway rat) | 310615 | Crtc2 |
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| DOID:418 | systemic scleroderma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | MGI:2143424 | Mus musculus (house mouse) | 215494 | Pomgnt2 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:10584 | retinitis pigmentosa | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:670 | amphetamine abuse | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:13608 | biliary atresia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:783 | end stage renal disease | MGI:106675 | Mus musculus (house mouse) | 11450 | Adipoq |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:1686 | glaucoma | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | RGD:631365 | Rattus norvegicus (Norway rat) | 297508 | Nampt |
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| DOID:418 | systemic scleroderma | RGD:3546 | Rattus norvegicus (Norway rat) | 25703 | Rbp4 |
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| DOID:1440 | Machado-Joseph disease | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:1059 | intellectual disability | RGD:2727 | Rattus norvegicus (Norway rat) | 292804 | Gpi |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:11714 | gestational diabetes | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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| DOID:8778 | Crohn's disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060639 | permanent neonatal diabetes mellitus | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:2018 | hyperinsulinism | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:1168 | familial hyperlipidemia | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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