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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:0060669 | cerebral cavernous malformation | HGNC:1737 | Homo sapiens (human) | 8476 | CDC42BPA |
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| DOID:14227 | azoospermia | HGNC:1737 | Homo sapiens (human) | 8476 | CDC42BPA |
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| DOID:0060041 | autism spectrum disorder | HGNC:28405 | Homo sapiens (human) | 84787 | KMT5C |
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| DOID:916 | liver benign neoplasm | HGNC:28405 | Homo sapiens (human) | 84787 | KMT5C |
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| DOID:0112232 | lissencephaly 3 | HGNC:20768 | Homo sapiens (human) | 84790 | TUBA1C |
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| DOID:0050453 | lissencephaly | HGNC:20768 | Homo sapiens (human) | 84790 | TUBA1C |
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| DOID:0112234 | microlissencephaly | HGNC:20768 | Homo sapiens (human) | 84790 | TUBA1C |
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| DOID:0080918 | polymicrogyria | HGNC:20768 | Homo sapiens (human) | 84790 | TUBA1C |
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| DOID:0111434 | optic atrophy 10 | HGNC:18647 | Homo sapiens (human) | 84816 | RTN4IP1 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:18358 | Homo sapiens (human) | 84818 | IL17RC |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0070202 | familial partial lipodystrophy type 2 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:3911 | progeria | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0080299 | partial lipodystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:423 | myopathy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:11726 | Emery-Dreifuss muscular dystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0070248 | autosomal recessive Emery-Dreifuss muscular dystrophy 3 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0110425 | dilated cardiomyopathy 1A | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:9884 | muscular dystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0111450 | progressive myoclonus epilepsy 9 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:8398 | osteoarthritis | HGNC:1980 | Homo sapiens (human) | 8483 | CILP |
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