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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:0111907 | thrombophilia due to thrombin defect | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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| DOID:2211 | factor XIII deficiency | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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| DOID:9477 | pulmonary embolism | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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| DOID:8947 | diabetic retinopathy | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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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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| DOID:5408 | Paget's disease of bone | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:3429 | inclusion body myositis | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0110168 | Charcot-Marie-Tooth disease type 2Y | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0060205 | frontotemporal dementia and/or amyotrophic lateral sclerosis 6 | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:1289 | neurodegenerative disease | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:9255 | frontotemporal dementia | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:1380 | endometrial cancer | MGI:1921405 | Mus musculus (house mouse) | 74155 | Errfi1 |
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| DOID:8398 | osteoarthritis | MGI:1921405 | Mus musculus (house mouse) | 74155 | Errfi1 |
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| DOID:906 | peroxisomal disease | MGI:1921409 | Mus musculus (house mouse) | 74159 | Acbd5 |
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| DOID:0080946 | retinal dystrophy with leukodystrophy | MGI:1921409 | Mus musculus (house mouse) | 74159 | Acbd5 |
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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:8466 | retinal degeneration | HGNC:12672 | Homo sapiens (human) | 7417 | VDAC2 |
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