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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:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:3068 | glioblastoma | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:5082 | liver cirrhosis | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:8947 | diabetic retinopathy | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:612 | primary immunodeficiency disease | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:0050211 | swine influenza | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:162 | cancer | HGNC:8997 | Homo sapiens (human) | 5305 | PIP4K2A |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:10941 | intracranial aneurysm | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0050770 | polycystic liver disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0080322 | polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0060340 | ciliopathy | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:3021 | acute kidney failure | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:8466 | retinal degeneration | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:10941 | intracranial aneurysm | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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