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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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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:0050545 | visceral heterotaxy | MGI:87912 | Mus musculus (house mouse) | 11481 | Acvr2b |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | MGI:1352630 | Mus musculus (house mouse) | 20928 | Abcc9 |
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| DOID:0050660 | Beare-Stevenson cutis gyrata syndrome | MGI:95523 | Mus musculus (house mouse) | 14183 | Fgfr2 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | MGI:1196466 | Mus musculus (house mouse) | 13511 | Dsg2 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | MGI:96673 | Mus musculus (house mouse) | 16509 | Kcne1 |
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| DOID:0060291 | oculodentodigital dysplasia | MGI:95713 | Mus musculus (house mouse) | 14609 | Gja1 |
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| DOID:0070069 | autosomal dominant intellectual developmental disorder 39 | MGI:1100511 | Mus musculus (house mouse) | 17933 | Myt1l |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | MGI:894698 | Mus musculus (house mouse) | 20391 | Sgca |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | MGI:1923097 | Mus musculus (house mouse) | 75847 | Crppa |
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| DOID:0050629 | Aicardi-Goutieres syndrome | MGI:1889575 | Mus musculus (house mouse) | 56417 | Adar |
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| DOID:0111149 | autosomal recessive isolated ectopia lentis 2 | MGI:2389008 | Mus musculus (house mouse) | 229595 | Adamtsl4 |
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| DOID:0111030 | hemochromatosis type 3 | MGI:1354956 | Mus musculus (house mouse) | 50765 | Tfr2 |
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| DOID:0110153 | Charcot-Marie-Tooth disease type 1E | MGI:97631 | Mus musculus (house mouse) | 18858 | Pmp22 |
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| DOID:0050632 | oculocutaneous albinism | MGI:98880 | Mus musculus (house mouse) | 22173 | Tyr |
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| DOID:14789 | spondyloepiphyseal dysplasia congenita | MGI:88452 | Mus musculus (house mouse) | 12824 | Col2a1 |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060041 | autism spectrum disorder | MGI:1298205 | Mus musculus (house mouse) | 20539 | Slc7a5 |
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| DOID:8354 | complement component 3 deficiency | MGI:88227 | Mus musculus (house mouse) | 12266 | C3 |
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| DOID:0111000 | Joubert syndrome 5 | MGI:2384917 | Mus musculus (house mouse) | 216274 | Cep290 |
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| DOID:4795 | GM2 gangliosidosis, AB variant | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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| DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | MGI:104903 | Mus musculus (house mouse) | 14734 | Gpc3 |
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| DOID:0110977 | brachydactyly type A1C | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:2377 | multiple sclerosis | MGI:97551 | Mus musculus (house mouse) | 18646 | Prf1 |
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| DOID:0060868 | leukoencephalopathy with vanishing white matter | MGI:2446176 | Mus musculus (house mouse) | 224045 | Eif2b5 |
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| DOID:0050955 | spinocerebellar ataxia type 2 | MGI:1277223 | Mus musculus (house mouse) | 20239 | Atxn2 |
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