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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:9884 | muscular dystrophy | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050453 | lissencephaly | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1432 | blindness | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1289 | neurodegenerative disease | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1432 | blindness | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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