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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:8577 | ulcerative colitis | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:841 | extrinsic allergic alveolitis | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:8505 | dermatitis herpetiformis | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:8717 | decubitus ulcer | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:6039 | uveal melanoma | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:11054 | urinary bladder cancer | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:0110540 | autosomal recessive nonsyndromic deafness 98 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:0111662 | ectodermal dysplasia 14 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:0050591 | tooth agenesis | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:8466 | retinal degeneration | HGNC:12674 | Homo sapiens (human) | 7419 | VDAC3 |
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| DOID:8466 | retinal degeneration | HGNC:12672 | Homo sapiens (human) | 7417 | VDAC2 |
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| DOID:11832 | visual epilepsy | HGNC:12672 | Homo sapiens (human) | 7417 | VDAC2 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:12672 | Homo sapiens (human) | 7417 | VDAC2 |
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| DOID:5844 | myocardial infarction | HGNC:12672 | Homo sapiens (human) | 7417 | VDAC2 |
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| DOID:11832 | visual epilepsy | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:10283 | prostate cancer | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:14330 | Parkinson's disease | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:8466 | retinal degeneration | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:0080855 | Parkinsonism | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0111385 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:1307 | dementia | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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