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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:13580 | cholestasis | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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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:9352 | type 2 diabetes mellitus | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:14330 | Parkinson's disease | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:9970 | obesity | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:2256 | osteochondrodysplasia | ZFIN:ZDB-GENE-080204-33 | Danio rerio (zebrafish) | 556800 | chst3b |
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| DOID:5419 | schizophrenia | ZFIN:ZDB-GENE-080204-33 | Danio rerio (zebrafish) | 556800 | chst3b |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | ZFIN:ZDB-GENE-080204-33 | Danio rerio (zebrafish) | 556800 | chst3b |
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| DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | ZFIN:ZDB-GENE-060307-1 | Danio rerio (zebrafish) | 557181 | alg13 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | ZFIN:ZDB-GENE-060929-1018 | Danio rerio (zebrafish) | 557187 | rxylt1 |
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| DOID:0050560 | Walker-Warburg syndrome | ZFIN:ZDB-GENE-060929-1018 | Danio rerio (zebrafish) | 557187 | rxylt1 |
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| DOID:1094 | attention deficit hyperactivity disorder | ZFIN:ZDB-GENE-041001-163 | Danio rerio (zebrafish) | 557218 | usta |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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