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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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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:3459 | breast carcinoma | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:12700 | hyperprolactinemia | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:162 | cancer | HGNC:11279 | Homo sapiens (human) | 6713 | SQLE |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:1094 | Homo sapiens (human) | 670 | BPHL |
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| DOID:0050571 | congenital disorder of glycosylation type II | MGI:1914217 | Mus musculus (house mouse) | 66967 | Edem3 |
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| DOID:4608 | common bile duct neoplasm | MGI:1914152 | Mus musculus (house mouse) | 66902 | Mtap |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | MGI:1914152 | Mus musculus (house mouse) | 66902 | Mtap |
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| DOID:1793 | pancreatic cancer | MGI:1914152 | Mus musculus (house mouse) | 66902 | Mtap |
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| DOID:0050625 | biliary tract benign neoplasm | MGI:1914152 | Mus musculus (house mouse) | 66902 | Mtap |
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| DOID:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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| DOID:0110658 | congenital myasthenic syndrome 15 | MGI:1914039 | Mus musculus (house mouse) | 66789 | Alg14 |
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| DOID:9743 | diabetic neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:83 | cataract | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1913498 | Mus musculus (house mouse) | 66248 | Alg5 |
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| DOID:0080322 | polycystic kidney disease | MGI:1913498 | Mus musculus (house mouse) | 66248 | Alg5 |
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| DOID:684 | hepatocellular carcinoma | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:10579 | leukodystrophy | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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