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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:11984 | hypertrophic cardiomyopathy | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:8466 | retinal degeneration | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:12930 | dilated cardiomyopathy | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:3312 | bipolar disorder | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:7998 | hyperthyroidism | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:0081292 | traumatic brain injury | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0070288 | primary autosomal recessive microcephaly 17 | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:10907 | microcephaly | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:11832 | visual epilepsy | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0070297 | primary microcephaly | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:1826 | epilepsy | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:8398 | osteoarthritis | HGNC:1980 | Homo sapiens (human) | 8483 | CILP |
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| DOID:9074 | systemic lupus erythematosus | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:2377 | multiple sclerosis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:5844 | myocardial infarction | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:11476 | osteoporosis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:13774 | Addison's disease | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:823 | periapical periodontitis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:5812 | MHC class II deficiency | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:7148 | rheumatoid arthritis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:0080236 | autosomal dominant intellectual developmental disorder 45 | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:150 | disease of mental health | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:3571 | liver cancer | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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| DOID:767 | muscular atrophy | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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