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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:0090034 | myoclonic dystonia 11 | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
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| DOID:10534 | stomach cancer | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
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| DOID:11446 | sciatic neuropathy | HGNC:1396 | Homo sapiens (human) | 8911 | CACNA1I |
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| DOID:5419 | schizophrenia | HGNC:1396 | Homo sapiens (human) | 8911 | CACNA1I |
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| DOID:1825 | childhood absence epilepsy | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:11446 | sciatic neuropathy | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:446 | primary hyperaldosteronism | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:0111742 | cerebellar ataxia type 42 | HGNC:1394 | Homo sapiens (human) | 8913 | CACNA1G |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:11813 | Homo sapiens (human) | 8914 | TIMELESS |
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| DOID:1574 | alcohol use disorder | HGNC:11813 | Homo sapiens (human) | 8914 | TIMELESS |
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| DOID:0081203 | autosomal recessive intellectual developmental disorder 38 | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:10123 | pigmentation disease | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:1826 | epilepsy | HGNC:1117 | Homo sapiens (human) | 8927 | BSN |
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| DOID:0050545 | visceral heterotaxy | HGNC:3814 | Homo sapiens (human) | 8928 | FOXH1 |
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| DOID:0060341 | agnathia-otocephaly complex | HGNC:3814 | Homo sapiens (human) | 8928 | FOXH1 |
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| DOID:6039 | uveal melanoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0080199 | colorectal carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:1324 | lung cancer | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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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:3635 | congenital myasthenic syndrome | HGNC:15963 | Homo sapiens (human) | 8973 | CHRNA6 |
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| DOID:809 | cocaine abuse | HGNC:15963 | Homo sapiens (human) | 8973 | CHRNA6 |
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| DOID:1574 | alcohol use disorder | HGNC:15963 | Homo sapiens (human) | 8973 | CHRNA6 |
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