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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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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:10534 | stomach cancer | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:3459 | breast carcinoma | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:0070154 | hereditary sensory neuropathy type 1F | HGNC:24526 | Homo sapiens (human) | 25923 | ATL3 |
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| DOID:0110791 | hereditary spastic paraplegia 3A | HGNC:24526 | Homo sapiens (human) | 25923 | ATL3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24526 | Homo sapiens (human) | 25923 | ATL3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24047 | Homo sapiens (human) | 64225 | ATL2 |
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| DOID:0110791 | hereditary spastic paraplegia 3A | HGNC:24047 | Homo sapiens (human) | 64225 | ATL2 |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:794 | Homo sapiens (human) | 471 | ATIC |
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| DOID:14330 | Parkinson's disease | HGNC:21899 | Homo sapiens (human) | 285973 | ATG9B |
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| DOID:14330 | Parkinson's disease | HGNC:22408 | Homo sapiens (human) | 79065 | ATG9A |
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| DOID:0080540 | galactosialidosis | SGD:S000000343 | Saccharomyces cerevisiae S288C | 852436 | ATG42 |
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| DOID:3211 | lysosomal storage disease | SGD:S000000343 | Saccharomyces cerevisiae S288C | 852436 | ATG42 |
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| DOID:10211 | cholelithiasis | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:3908 | lung non-small cell carcinoma | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:1793 | pancreatic cancer | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:1380 | endometrial cancer | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:9744 | type 1 diabetes mellitus | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:8692 | myeloid leukemia | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:2394 | ovarian cancer | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:3803 | Crigler-Najjar syndrome | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:2739 | Gilbert syndrome | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:8778 | Crohn's disease | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:4988 | alcoholic pancreatitis | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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