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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:6432 | pulmonary hypertension | MGI:1915146 | Mus musculus (house mouse) | 67896 | Ccdc80 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | MGI:1915164 | Mus musculus (house mouse) | 67914 | Coq9 |
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| DOID:0070242 | primary coenzyme Q10 deficiency 5 | MGI:1915164 | Mus musculus (house mouse) | 67914 | Coq9 |
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| DOID:1206 | Rett syndrome | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:0080467 | developmental and epileptic encephalopathy 2 | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:11832 | visual epilepsy | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:1059 | intellectual disability | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:13372 | alpha 1-antitrypsin deficiency | MGI:1915181 | Mus musculus (house mouse) | 67931 | Serpini2 |
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| DOID:0060479 | Shwachman-Diamond syndrome | MGI:1915181 | Mus musculus (house mouse) | 67931 | Serpini2 |
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| DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | MGI:1915181 | Mus musculus (house mouse) | 67931 | Serpini2 |
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| DOID:1682 | congenital heart disease | MGI:1915183 | Mus musculus (house mouse) | 67933 | Hcfc2 |
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| DOID:0111849 | osteogenesis imperfecta type 20 | MGI:1891421 | Mus musculus (house mouse) | 67943 | Mesd |
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| DOID:0112227 | tubulinopathy | MGI:1915201 | Mus musculus (house mouse) | 67951 | Tubb6 |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | MGI:1915201 | Mus musculus (house mouse) | 67951 | Tubb6 |
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| DOID:13934 | facial paralysis | MGI:1915201 | Mus musculus (house mouse) | 67951 | Tubb6 |
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| DOID:0060260 | ptosis | MGI:1915201 | Mus musculus (house mouse) | 67951 | Tubb6 |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | MGI:1915201 | Mus musculus (house mouse) | 67951 | Tubb6 |
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| DOID:14504 | Niemann-Pick disease | MGI:1915213 | Mus musculus (house mouse) | 67963 | Npc2 |
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| DOID:0070114 | Niemann-Pick disease type C2 | MGI:1915213 | Mus musculus (house mouse) | 67963 | Npc2 |
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| DOID:5419 | schizophrenia | RGD:1585921 | Rattus norvegicus (Norway rat) | 679668 | LRRTM1 |
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| DOID:14330 | Parkinson's disease | MGI:1915221 | Mus musculus (house mouse) | 67971 | Tppp3 |
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| DOID:10763 | hypertension | MGI:104653 | Mus musculus (house mouse) | 67972 | Atp2b1 |
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| DOID:10591 | pre-eclampsia | MGI:104653 | Mus musculus (house mouse) | 67972 | Atp2b1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | MGI:104653 | Mus musculus (house mouse) | 67972 | Atp2b1 |
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| DOID:11714 | gestational diabetes | MGI:104653 | Mus musculus (house mouse) | 67972 | Atp2b1 |
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