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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:83 | cataract | HGNC:6610 | Homo sapiens (human) | 3982 | LIM2 |
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| DOID:10763 | hypertension | RGD:3249 | Rattus norvegicus (Norway rat) | 24617 | Serpine1 |
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| DOID:0080490 | mucolipidosis type IV | WB:WBGene00000846 | Caenorhabditis elegans | 176074 | cup-5 |
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| DOID:2236 | congenital afibrinogenemia | MGI:95526 | Mus musculus (house mouse) | 99571 | Fgg |
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| DOID:9970 | obesity | HGNC:6931 | Homo sapiens (human) | 4159 | MC3R |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:10763 | hypertension | RGD:3186 | Rattus norvegicus (Norway rat) | 24600 | Nos3 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:7160 | Homo sapiens (human) | 4323 | MMP14 |
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| DOID:10588 | adrenoleukodystrophy | MGI:1349215 | Mus musculus (house mouse) | 11666 | Abcd1 |
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| DOID:3210 | Pelizaeus-Merzbacher disease | MGI:97623 | Mus musculus (house mouse) | 18823 | Plp1 |
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| DOID:0050440 | familial partial lipodystrophy | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:10584 | retinitis pigmentosa | FB:FBgn0259685 | Drosophila melanogaster (fruit fly) | 42896 | crb |
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| DOID:14791 | Leber congenital amaurosis | FB:FBgn0259685 | Drosophila melanogaster (fruit fly) | 42896 | crb |
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| DOID:10652 | Alzheimer's disease | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:10763 | hypertension | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0050464 | Farber lipogranulomatosis | MGI:1277124 | Mus musculus (house mouse) | 11886 | Asah1 |
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| DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | MGI:98864 | Mus musculus (house mouse) | 22138 | Ttn |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:3144 | cutis laxa | MGI:1346091 | Mus musculus (house mouse) | 23876 | Fbln5 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:5419 | schizophrenia | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | MGI:96257 | Mus musculus (house mouse) | 15530 | Hspg2 |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | MGI:96257 | Mus musculus (house mouse) | 15530 | Hspg2 |
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