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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:8398 | osteoarthritis | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:11714 | gestational diabetes | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:8947 | diabetic retinopathy | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:10283 | prostate cancer | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0111108 | maturity-onset diabetes of the young type 10 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:2018 | hyperinsulinism | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:4947 | cholangiocarcinoma | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:10652 | Alzheimer's disease | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:1793 | pancreatic cancer | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:9351 | diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:1920 | hyperuricemia | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0080573 | congenital disorder of glycosylation Ix | RGD:1311563 | Rattus norvegicus (Norway rat) | 363160 | Stt3b |
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| DOID:0080572 | congenital disorder of glycosylation Iw | RGD:1311563 | Rattus norvegicus (Norway rat) | 363160 | Stt3b |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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| DOID:10763 | hypertension | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:9970 | obesity | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:13359 | Ehlers-Danlos syndrome | RGD:1309214 | Rattus norvegicus (Norway rat) | 364675 | B4galt7 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | RGD:1309214 | Rattus norvegicus (Norway rat) | 364675 | B4galt7 |
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| DOID:3534 | Lafora disease | RGD:735081 | Rattus norvegicus (Norway rat) | 364682 | Nhlrc1 |
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| DOID:9351 | diabetes mellitus | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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