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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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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:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16142 | Homo sapiens (human) | 79144 | PPDPF |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:11724 | limb-girdle muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:12930 | dilated cardiomyopathy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:1826 | epilepsy | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:0110786 | hereditary spastic paraplegia 35 | HGNC:21197 | Homo sapiens (human) | 79152 | FA2H |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080488 | mucolipidosis | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:13918 | Homo sapiens (human) | 7916 | PRRC2A |
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| DOID:1289 | neurodegenerative disease | ZFIN:ZDB-GENE-040513-2 | Danio rerio (zebrafish) | 791696 | asic1a |
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| DOID:14452 | hypokalemic periodic paralysis | ZFIN:ZDB-GENE-040513-2 | Danio rerio (zebrafish) | 791696 | asic1a |
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| DOID:326 | ischemia | ZFIN:ZDB-GENE-040513-2 | Danio rerio (zebrafish) | 791696 | asic1a |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:13919 | Homo sapiens (human) | 7917 | BAG6 |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:13919 | Homo sapiens (human) | 7917 | BAG6 |
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| DOID:8398 | osteoarthritis | HGNC:13919 | Homo sapiens (human) | 7917 | BAG6 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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