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GlyTouCan
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:0050633 | ocular albinism 1 | MGI:107193 | Mus musculus (house mouse) | 18241 | Gpr143 |
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| DOID:1919 | Lesch-Nyhan syndrome | MGI:96217 | Mus musculus (house mouse) | 15452 | Hprt1 |
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| DOID:0050958 | spinocerebellar ataxia type 7 | MGI:2179277 | Mus musculus (house mouse) | 246103 | Atxn7 |
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| DOID:0112306 | Mahvash Disease | MGI:99572 | Mus musculus (house mouse) | 14527 | Gcgr |
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| DOID:0080439 | developmental and epileptic encephalopathy 14 | MGI:1924627 | Mus musculus (house mouse) | 227632 | Kcnt1 |
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| DOID:11119 | Gilles de la Tourette syndrome | MGI:2679446 | Mus musculus (house mouse) | 76965 | Slitrk1 |
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| DOID:3529 | congenital myopathy 1A | MGI:99659 | Mus musculus (house mouse) | 20190 | Ryr1 |
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| DOID:0080350 | retinitis pigmentosa 77 | MGI:1917585 | Mus musculus (house mouse) | 70335 | Reep6 |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | MGI:2447586 | Mus musculus (house mouse) | 243853 | Fkrp |
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| DOID:0110175 | Charcot-Marie-Tooth disease axonal type 2O | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0080089 | tubular aggregate myopathy 1 | MGI:107476 | Mus musculus (house mouse) | 20866 | Stim1 |
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| DOID:0081169 | Leber congenital amaurosis 19 | MGI:101850 | Mus musculus (house mouse) | 77593 | Usp45 |
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| DOID:0110868 | congenital stationary night blindness 1D | MGI:2384871 | Mus musculus (house mouse) | 214111 | Slc24a1 |
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| DOID:3263 | piebaldism | MGI:96677 | Mus musculus (house mouse) | 16590 | Kit |
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| DOID:12930 | dilated cardiomyopathy | MGI:95410 | Mus musculus (house mouse) | 13866 | Erbb2 |
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| DOID:0111725 | geleophysic dysplasia 1 | MGI:1925044 | Mus musculus (house mouse) | 77794 | Adamtsl2 |
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| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | MGI:88447 | Mus musculus (house mouse) | 12815 | Col11a2 |
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| DOID:3322 | GM1 gangliosidosis | MGI:88151 | Mus musculus (house mouse) | 12091 | Glb1 |
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| DOID:14264 | benign neonatal seizures | MGI:1336181 | Mus musculus (house mouse) | 110862 | Kcnq3 |
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| DOID:12120 | pulmonary alveolar proteinosis | MGI:1339754 | Mus musculus (house mouse) | 12982 | Csf2ra |
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| DOID:0080092 | myofibrillar myopathy 1 | MGI:94885 | Mus musculus (house mouse) | 13346 | Des |
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| DOID:0110372 | retinitis pigmentosa 4 | MGI:97914 | Mus musculus (house mouse) | 212541 | Rho |
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| DOID:5408 | Paget's disease of bone | MGI:1314891 | Mus musculus (house mouse) | 21934 | Tnfrsf11a |
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| DOID:83 | cataract | MGI:104698 | Mus musculus (house mouse) | 233187 | Lim2 |
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| DOID:0110567 | autosomal dominant nonsyndromic deafness 41 | MGI:2665170 | Mus musculus (house mouse) | 231602 | P2rx2 |
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