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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:9256 | colorectal cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:10534 | stomach cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:169 | neuroendocrine tumor | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:4971 | myelofibrosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:684 | hepatocellular carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:8955 | sideroblastic anemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3910 | lung adenocarcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:2224 | essential thrombocythemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:9970 | obesity | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:0080108 | myoglobinuria | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:0080108 | myoglobinuria | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:9970 | obesity | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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| DOID:2566 | corneal dystrophy | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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