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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
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:3083 | chronic obstructive pulmonary disease | HGNC:216 | Homo sapiens (human) | 8754 | ADAM9 |
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| DOID:162 | cancer | HGNC:1801 | Homo sapiens (human) | 8760 | CDS2 |
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| DOID:0110587 | autosomal dominant nonsyndromic deafness 66 | HGNC:1632 | Homo sapiens (human) | 8763 | CD164 |
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| DOID:5844 | myocardial infarction | HGNC:11912 | Homo sapiens (human) | 8764 | TNFRSF14 |
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| DOID:2349 | arteriosclerosis | HGNC:11912 | Homo sapiens (human) | 8764 | TNFRSF14 |
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| DOID:10155 | intestinal cancer | HGNC:9760 | Homo sapiens (human) | 8766 | RAB11A |
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| DOID:0050589 | inflammatory bowel disease | HGNC:9760 | Homo sapiens (human) | 8766 | RAB11A |
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| DOID:612 | primary immunodeficiency disease | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:11132 | prostatic hypertrophy | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:3525 | middle cerebral artery infarction | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:9119 | acute myeloid leukemia | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:1596 | depressive disorder | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:2560 | morphine dependence | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:10652 | Alzheimer's disease | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:1240 | leukemia | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:14221 | abdominal obesity-metabolic syndrome 1 | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:224 | transient cerebral ischemia | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:10763 | hypertension | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:0060108 | brain glioma | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:9970 | obesity | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:423 | myopathy | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:10908 | hydrocephalus | HGNC:7208 | Homo sapiens (human) | 8777 | MPDZ |
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| DOID:11168 | anogenital venereal wart | HGNC:11914 | Homo sapiens (human) | 8784 | TNFRSF18 |
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