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GlyTouCan
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
LM-GlycoRepo
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:0111272 | occipital horn syndrome | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:2237 | hepatitis | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:684 | hepatocellular carcinoma | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:893 | Wilson disease | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:896 | metal metabolism disorder | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:12377 | spinal muscular atrophy | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:3459 | breast carcinoma | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:1838 | Menkes disease | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:3144 | cutis laxa | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:3627 | aortic aneurysm | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:0111196 | X-linked distal spinal muscular atrophy 3 | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:12377 | spinal muscular atrophy | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:11758 | iron deficiency anemia | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:10652 | Alzheimer's disease | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:0111272 | occipital horn syndrome | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:893 | Wilson disease | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:1838 | Menkes disease | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:8398 | osteoarthritis | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:896 | metal metabolism disorder | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:0070140 | autosomal recessive cutis laxa type IIC | HGNC:857 | Homo sapiens (human) | 529 | ATP6V1E1 |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:1432 | blindness | HGNC:863 | Homo sapiens (human) | 8992 | ATP6V0E1 |
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| DOID:1059 | intellectual disability | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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