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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:684 | hepatocellular carcinoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:3571 | liver cancer | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:13603 | obstructive jaundice | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:224 | transient cerebral ischemia | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:11446 | sciatic neuropathy | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:2154 | nephroblastoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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| DOID:1826 | epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080768 | pyridoxine-dependent epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0014667 | disease of metabolism | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0014667 | disease of metabolism | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:8466 | retinal degeneration | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8808 | Homo sapiens (human) | 5162 | PDHB |
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| DOID:0110011 | advanced sleep phase syndrome 1 | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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