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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:0050650 | familial atrial fibrillation | MGI:106921 | Mus musculus (house mouse) | 72821 | Scn2b |
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| DOID:11832 | visual epilepsy | MGI:106921 | Mus musculus (house mouse) | 72821 | Scn2b |
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| DOID:0111351 | D-2-hydroxyglutaric aciduria 1 | HGNC:28358 | Homo sapiens (human) | 728294 | D2HGDH |
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| DOID:0050679 | blue cone monochromacy | HGNC:26952 | Homo sapiens (human) | 728458 | OPN1MW2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:32035 | Homo sapiens (human) | 728577 | CNTNAP3B |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:32035 | Homo sapiens (human) | 728577 | CNTNAP3B |
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| DOID:2921 | glomerulonephritis | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:783 | end stage renal disease | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:576 | proteinuria | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:0060299 | complement component 6 deficiency | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:6419 | tetralogy of Fallot | HGNC:4916 | Homo sapiens (human) | 7290 | HIRA |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:4916 | Homo sapiens (human) | 7290 | HIRA |
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| DOID:0050888 | syndromic intellectual disability | HGNC:23467 | Homo sapiens (human) | 729092 | AGAP5 |
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| DOID:1969 | cerebral palsy | HGNC:23467 | Homo sapiens (human) | 729092 | AGAP5 |
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| DOID:12960 | acrocephalosyndactylia | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:2340 | craniosynostosis | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:3459 | breast carcinoma | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:14768 | Saethre-Chotzen syndrome | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:1612 | breast cancer | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:6432 | pulmonary hypertension | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:0050827 | rheumatic heart disease | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:0080538 | Sweeney-Cox syndrome | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:11934 | Homo sapiens (human) | 7292 | TNFSF4 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:11934 | Homo sapiens (human) | 7292 | TNFSF4 |
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