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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2945 | severe acute respiratory syndrome | Xenbase:XB-GENE-5962623 | Xenopus laevis (African clawed frog) | 495825 | abo.3.L |
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| DOID:552 | pneumonia | Xenbase:XB-GENE-5962623 | Xenopus laevis (African clawed frog) | 495825 | abo.3.L |
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| DOID:4948 | gallbladder carcinoma | Xenbase:XB-GENE-5962623 | Xenopus laevis (African clawed frog) | 495825 | abo.3.L |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | Xenbase:XB-GENE-984410 | Xenopus laevis (African clawed frog) | 496338 | pomk.L |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | Xenbase:XB-GENE-984410 | Xenopus laevis (African clawed frog) | 496338 | pomk.L |
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| DOID:0060256 | Dowling-Degos disease | Xenbase:XB-GENE-979243 | Xenopus tropicalis (tropical clawed frog) | 496411 | pofut1 |
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| DOID:12716 | newborn respiratory distress syndrome | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:3827 | congenital diaphragmatic hernia | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:11198 | DiGeorge syndrome | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:1059 | intellectual disability | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:0060041 | autism spectrum disorder | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:14227 | azoospermia | Xenbase:XB-GENE-955052 | Xenopus tropicalis (tropical clawed frog) | 496577 | ndst1 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | Xenbase:XB-GENE-973748 | Xenopus tropicalis (tropical clawed frog) | 496628 | pomgnt2 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | Xenbase:XB-GENE-973748 | Xenopus tropicalis (tropical clawed frog) | 496628 | pomgnt2 |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | Xenbase:XB-GENE-1012156 | Xenopus tropicalis (tropical clawed frog) | 496641 | b3galnt2 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:9669 | senile cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:11714 | gestational diabetes | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:1793 | pancreatic cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0002116 | pterygium | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:2237 | hepatitis | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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