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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:0080230 | autosomal dominant intellectual developmental disorder 54 | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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| DOID:3525 | middle cerebral artery infarction | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| 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:5419 | schizophrenia | HGNC:17938 | Homo sapiens (human) | 50632 | CALY |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:17938 | Homo sapiens (human) | 50632 | CALY |
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| DOID:0080199 | colorectal carcinoma | HGNC:1458 | Homo sapiens (human) | 813 | CALU |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:1458 | Homo sapiens (human) | 813 | CALU |
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| DOID:14330 | Parkinson's disease | HGNC:20407 | Homo sapiens (human) | 125972 | CALR3 |
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| DOID:6000 | congestive heart failure | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:2394 | ovarian cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:8955 | sideroblastic anemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3910 | lung adenocarcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:9119 | acute myeloid leukemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:9256 | colorectal cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:2224 | essential thrombocythemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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