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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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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:3312 | bipolar disorder | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0060041 | autism spectrum disorder | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:10273 | heart conduction disease | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:10652 | Alzheimer's disease | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:224 | transient cerebral ischemia | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:3070 | high grade glioma | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0081224 | autosomal recessive intellectual developmental disorder 63 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:9277 | primary cerebellar degeneration | MGI:1932040 | Mus musculus (house mouse) | 81500 | Sil1 |
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| DOID:0080195 | Marinesco-Sjogren syndrome | MGI:1932040 | Mus musculus (house mouse) | 81500 | Sil1 |
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| DOID:6432 | pulmonary hypertension | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:0050787 | juvenile polyposis syndrome | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:384 | Wolff-Parkinson-White syndrome | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:14289 | Ebstein anomaly | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:0060389 | chromosome 10q23 deletion syndrome | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:8398 | osteoarthritis | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:5295 | intestinal disease | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:0111686 | hereditary mixed polyposis syndrome 2 | RGD:70989 | Rattus norvegicus (Norway rat) | 81507 | Bmpr1a |
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| DOID:3770 | pulmonary fibrosis | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:1826 | epilepsy | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:10763 | hypertension | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:5844 | myocardial infarction | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:9743 | diabetic neuropathy | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:11713 | diabetic angiopathy | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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| DOID:4483 | rhinitis | RGD:620401 | Rattus norvegicus (Norway rat) | 81509 | Bdkrb1 |
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