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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:0110192 | Charcot-Marie-Tooth disease type 4H | HGNC:16027 | Homo sapiens (human) | 89846 | FGD3 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16027 | Homo sapiens (human) | 89846 | FGD3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9083 | Homo sapiens (human) | 8985 | PLOD3 |
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| DOID:1459 | hypothyroidism | HGNC:9083 | Homo sapiens (human) | 8985 | PLOD3 |
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| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
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| DOID:0070355 | overactive bladder syndrome | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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| DOID:2841 | asthma | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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| DOID:0111729 | familial episodic pain syndrome 1 | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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| DOID:9743 | diabetic neuropathy | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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| DOID:1432 | blindness | HGNC:863 | Homo sapiens (human) | 8992 | ATP6V0E1 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:21624 | Homo sapiens (human) | 89953 | KLC4 |
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| DOID:1826 | epilepsy | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:3393 | coronary artery disease | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:12720 | cerebral atherosclerosis | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:3526 | cerebral infarction | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:1793 | pancreatic cancer | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:13641 | exfoliation syndrome | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:13129 | severe pre-eclampsia | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:13374 | fibrodysplasia ossificans progressiva | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:10273 | heart conduction disease | HGNC:18863 | Homo sapiens (human) | 90134 | KCNH7 |
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| DOID:1826 | epilepsy | HGNC:18863 | Homo sapiens (human) | 90134 | KCNH7 |
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| DOID:2843 | long QT syndrome | HGNC:18863 | Homo sapiens (human) | 90134 | KCNH7 |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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