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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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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:0110266 | cataract 9 multiple types | MGI:88515 | Mus musculus (house mouse) | 12954 | Cryaa |
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| DOID:10763 | hypertension | RGD:69051 | Rattus norvegicus (Norway rat) | 59086 | Tgfb1 |
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| DOID:0080056 | achondrogenesis type II | MGI:88452 | Mus musculus (house mouse) | 12824 | Col2a1 |
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| DOID:13580 | cholestasis | RGD:620248 | Rattus norvegicus (Norway rat) | 24891 | Abcb4 |
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| DOID:3310 | atopic dermatitis | MGI:96556 | Mus musculus (house mouse) | 16189 | Il4 |
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| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | MGI:88447 | Mus musculus (house mouse) | 12815 | Col11a2 |
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| DOID:0080026 | otospondylomegaepiphyseal dysplasia, autosomal recessive | MGI:88447 | Mus musculus (house mouse) | 12815 | Col11a2 |
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| DOID:6000 | congestive heart failure | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:10763 | hypertension | HGNC:9844 | Homo sapiens (human) | 10266 | RAMP2 |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | MGI:895149 | Mus musculus (house mouse) | 11370 | Acadvl |
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| DOID:5844 | myocardial infarction | HGNC:7097 | Homo sapiens (human) | 4282 | MIF |
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| DOID:2841 | asthma | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:13141 | uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3070 | high grade glioma | RGD:2194 | Rattus norvegicus (Norway rat) | 25393 | Bcan |
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| DOID:10763 | hypertension | RGD:621159 | Rattus norvegicus (Norway rat) | 60582 | Il1rn |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:14504 | Niemann-Pick disease | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
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| DOID:10763 | hypertension | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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| DOID:9074 | systemic lupus erythematosus | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0110939 | autosomal recessive osteopetrosis 5 | MGI:2655574 | Mus musculus (house mouse) | 14628 | Ostm1 |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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| DOID:0110646 | long QT syndrome 3 | MGI:98251 | Mus musculus (house mouse) | 20271 | Scn5a |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:0111064 | autosomal recessive distal hereditary motor neuronopathy 1 | HGNC:5542 | Homo sapiens (human) | 3508 | IGHMBP2 |
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