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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:10303 | sialadenitis | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:813 | septic arthritis | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:0112277 | immunodeficiency 79 | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:0080600 | COVID-19 | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:162 | cancer | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:13054 | Homo sapiens (human) | 9203 | ZMYM3 |
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| DOID:0050741 | alcohol dependence | HGNC:16437 | Homo sapiens (human) | 92086 | GGTLC1 |
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| DOID:5022 | aflatoxins-related hepatocellular carcinoma | HGNC:16437 | Homo sapiens (human) | 92086 | GGTLC1 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:0080494 | ovarian dysgenesis 2 | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:7725 | epilepsy with generalized tonic-clonic seizures | HGNC:6572 | Homo sapiens (human) | 9211 | LGI1 |
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| DOID:0060748 | familial temporal lobe epilepsy 1 | HGNC:6572 | Homo sapiens (human) | 9211 | LGI1 |
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| DOID:1826 | epilepsy | HGNC:6572 | Homo sapiens (human) | 9211 | LGI1 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:1319 | brain cancer | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:2871 | endometrial carcinoma | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:684 | hepatocellular carcinoma | HGNC:29608 | Homo sapiens (human) | 92140 | MTDH |
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| DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:11727 | facioscapulohumeral muscular dystrophy | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0081301 | intellectual developmental disorder with ocular anomalies and distinctive facial features | HGNC:25094 | Homo sapiens (human) | 92154 | MTSS2 |
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