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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:653 | purine-pyrimidine metabolic disorder | MGI:1298388 | Mus musculus (house mouse) | 22247 | Umps |
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| DOID:0050833 | orotic aciduria | MGI:1298388 | Mus musculus (house mouse) | 22247 | Umps |
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| DOID:11702 | dysgammaglobulinemia | MGI:109352 | Mus musculus (house mouse) | 22256 | Ung |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | MGI:109352 | Mus musculus (house mouse) | 22256 | Ung |
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| DOID:3525 | middle cerebral artery infarction | MGI:1097668 | Mus musculus (house mouse) | 22271 | Upp1 |
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| DOID:1287 | cardiovascular system disease | MGI:99542 | Mus musculus (house mouse) | 22278 | Usf1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:99542 | Mus musculus (house mouse) | 22278 | Usf1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2385025 | Mus musculus (house mouse) | 223774 | Alg12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | MGI:2385025 | Mus musculus (house mouse) | 223774 | Alg12 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:403 | Homo sapiens (human) | 224 | ALDH3A2 |
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| DOID:0060256 | Dowling-Degos disease | MGI:2444232 | Mus musculus (house mouse) | 224143 | Poglut1 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | MGI:2444232 | Mus musculus (house mouse) | 224143 | Poglut1 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | MGI:2444232 | Mus musculus (house mouse) | 224143 | Poglut1 |
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| DOID:14735 | hereditary angioedema | MGI:1919192 | Mus musculus (house mouse) | 226101 | Myof |
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| DOID:11724 | limb-girdle muscular dystrophy | MGI:1919192 | Mus musculus (house mouse) | 226101 | Myof |
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| DOID:417 | autoimmune disease | MGI:104803 | Mus musculus (house mouse) | 22619 | Siae |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:5138 | leiomyomatosis | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0081097 | Rafiq syndrome | MGI:2684954 | Mus musculus (house mouse) | 227619 | Man1b1 |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:9869 | hereditary fructose intolerance syndrome | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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