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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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MIRAGE
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:0110423 | dilated cardiomyopathy 1C | MGI:1344412 | Mus musculus (house mouse) | 24131 | Ldb3 |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | MGI:88123 | Mus musculus (house mouse) | 12000 | Avpr2 |
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| DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | MGI:1914047 | Mus musculus (house mouse) | 66797 | Cntnap2 |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | MGI:1306775 | Mus musculus (house mouse) | 20916 | Sucla2 |
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| DOID:0060747 | Duane-radial ray syndrome | MGI:2139360 | Mus musculus (house mouse) | 99377 | Sall4 |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | MGI:1890773 | Mus musculus (house mouse) | 60595 | Actn4 |
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| DOID:0050474 | Netherton syndrome | MGI:1919682 | Mus musculus (house mouse) | 72432 | Spink5 |
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| DOID:0050328 | congenital hypothyroidism | MGI:98813 | Mus musculus (house mouse) | 22018 | Tpo |
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| DOID:0111001 | Joubert syndrome 6 | MGI:1923928 | Mus musculus (house mouse) | 329795 | Tmem67 |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | MGI:2444341 | Mus musculus (house mouse) | 320595 | Phf8 |
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| DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | MGI:103067 | Mus musculus (house mouse) | 22589 | Atrx |
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| DOID:0060877 | bullous congenital ichthyosiform erythroderma | MGI:96699 | Mus musculus (house mouse) | 16681 | Krt2 |
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| DOID:0070055 | Xia-Gibbs Syndrome | MGI:2444218 | Mus musculus (house mouse) | 230793 | Ahdc1 |
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| DOID:0080181 | PHARC syndrome | MGI:1923442 | Mus musculus (house mouse) | 76192 | Abhd12 |
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| DOID:0050144 | Kartagener syndrome | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:0050453 | lissencephaly | MGI:101864 | Mus musculus (house mouse) | 13138 | Dag1 |
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| DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | MGI:2679449 | Mus musculus (house mouse) | 245450 | Slitrk2 |
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| DOID:0090053 | episodic kinesigenic dyskinesia 1 | MGI:1916267 | Mus musculus (house mouse) | 69017 | Prrt2 |
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| DOID:0060861 | microphthalmia with limb anomalies | MGI:1929878 | Mus musculus (house mouse) | 64075 | Smoc1 |
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| DOID:2841 | asthma | MGI:105367 | Mus musculus (house mouse) | 16190 | Il4ra |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:109334 | Mus musculus (house mouse) | 384783 | Irs2 |
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| DOID:12347 | osteogenesis imperfecta | MGI:88468 | Mus musculus (house mouse) | 12843 | Col1a2 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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| DOID:0110969 | brachydactyly type B1 | MGI:1347521 | Mus musculus (house mouse) | 26564 | Ror2 |
|
