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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:2154 | nephroblastoma | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:1206 | Rett syndrome | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:0080467 | developmental and epileptic encephalopathy 2 | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:11832 | visual epilepsy | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:1059 | intellectual disability | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:11714 | gestational diabetes | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:8947 | diabetic retinopathy | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:9351 | diabetes mellitus | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:1779 | Homo sapiens (human) | 1024 | CDK8 |
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| DOID:0112221 | developmental and epileptic encephalopathy 87 | HGNC:1779 | Homo sapiens (human) | 1024 | CDK8 |
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| DOID:9993 | hypoglycemia | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:0050593 | primary congenital glaucoma | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:10652 | Alzheimer's disease | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:1612 | breast cancer | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:10825 | essential hypertension | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:0050569 | Seckel syndrome | HGNC:18672 | Homo sapiens (human) | 55755 | CDK5RAP2 |
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| DOID:0070286 | primary autosomal recessive microcephaly 3 | HGNC:18672 | Homo sapiens (human) | 55755 | CDK5RAP2 |
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| DOID:10907 | microcephaly | HGNC:18672 | Homo sapiens (human) | 55755 | CDK5RAP2 |
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| DOID:0050453 | lissencephaly | HGNC:1776 | Homo sapiens (human) | 8941 | CDK5R2 |
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| DOID:1826 | epilepsy | HGNC:1776 | Homo sapiens (human) | 8941 | CDK5R2 |
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| DOID:8725 | vascular dementia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:10652 | Alzheimer's disease | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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