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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:14330 | Parkinson's disease | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:8725 | vascular dementia | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:3312 | bipolar disorder | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:5419 | schizophrenia | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:12217 | Lewy body dementia | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:3192 | neurilemmoma | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:4752 | multiple system atrophy | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:8692 | myeloid leukemia | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:10652 | Alzheimer's disease | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:1596 | depressive disorder | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:11870 | Pick's disease | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:3981 | pantothenate kinase-associated neurodegeneration | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
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| DOID:0060337 | CEDNIK syndrome | HGNC:11133 | Homo sapiens (human) | 9342 | SNAP29 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:11133 | Homo sapiens (human) | 9342 | SNAP29 |
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| DOID:0110683 | congenital myasthenic syndrome 18 | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:9970 | obesity | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:14250 | Down syndrome | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:5419 | schizophrenia | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:9655 | oral mucosa leukoplakia | HGNC:11128 | Homo sapiens (human) | 6615 | SNAI1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11128 | Homo sapiens (human) | 6615 | SNAI1 |
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| DOID:4159 | skin cancer | HGNC:11128 | Homo sapiens (human) | 6615 | SNAI1 |
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| DOID:9256 | colorectal cancer | HGNC:11128 | Homo sapiens (human) | 6615 | SNAI1 |
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| DOID:305 | carcinoma | HGNC:11128 | Homo sapiens (human) | 6615 | SNAI1 |
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