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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:0050683 | Bothnia retinal dystrophy | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:0111015 | Newfoundland cone-rod dystrophy | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:11105 | fundus albipunctatus | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10021 | Homo sapiens (human) | 11035 | RIPK3 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:10021 | Homo sapiens (human) | 11035 | RIPK3 |
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| DOID:1749 | squamous cell carcinoma | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:0111952 | immunodeficiency 57 | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:9201 | lichen planus | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:1826 | epilepsy | HGNC:10019 | Homo sapiens (human) | 8737 | RIPK1 |
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| DOID:162 | cancer | HGNC:10018 | Homo sapiens (human) | 6015 | RING1 |
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| DOID:0060037 | developmental disorder of mental health | HGNC:10018 | Homo sapiens (human) | 6015 | RING1 |
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| DOID:0070416 | Luo-Schoch-Yamamoto syndrome | HGNC:10018 | Homo sapiens (human) | 6015 | RING1 |
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| DOID:0110713 | Oguchi disease-2 | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:1574 | alcohol use disorder | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:6000 | congestive heart failure | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:5679 | retinal disease | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:8499 | night blindness | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:11105 | fundus albipunctatus | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:0110862 | congenital stationary night blindness autosomal dominant 1 | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:0110372 | retinitis pigmentosa 4 | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:10584 | retinitis pigmentosa | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:8499 | night blindness | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10011 | Homo sapiens (human) | 6009 | RHEB |
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| DOID:13515 | tuberous sclerosis | HGNC:10011 | Homo sapiens (human) | 6009 | RHEB |
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