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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:9248 | Pallister-Hall syndrome | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
|
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| DOID:11836 | clubfoot | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:13714 | anodontia | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
|
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| DOID:11193 | syndactyly | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
|
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| DOID:178 | vascular disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
|
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| DOID:783 | end stage renal disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:8947 | diabetic retinopathy | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:12849 | autistic disorder | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
|
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| DOID:10763 | hypertension | HGNC:4324 | Homo sapiens (human) | 2740 | GLP1R |
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| DOID:1574 | alcohol use disorder | HGNC:4324 | Homo sapiens (human) | 2740 | GLP1R |
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| DOID:4195 | hyperglycemia | HGNC:4324 | Homo sapiens (human) | 2740 | GLP1R |
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| DOID:9970 | obesity | HGNC:4324 | Homo sapiens (human) | 2740 | GLP1R |
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| DOID:0060696 | hyperekplexia 1 | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0060695 | hyperekplexia | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | HGNC:4327 | Homo sapiens (human) | 2742 | GLRA2 |
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| DOID:0060697 | hyperekplexia 2 | HGNC:4329 | Homo sapiens (human) | 2743 | GLRB |
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| DOID:0112207 | developmental and epileptic encephalopathy 71 | HGNC:4331 | Homo sapiens (human) | 2744 | GLS |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:4331 | Homo sapiens (human) | 2744 | GLS |
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| DOID:9970 | obesity | HGNC:4330 | Homo sapiens (human) | 2745 | GLRX |
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| DOID:224 | transient cerebral ischemia | HGNC:4330 | Homo sapiens (human) | 2745 | GLRX |
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| DOID:14330 | Parkinson's disease | HGNC:4330 | Homo sapiens (human) | 2745 | GLRX |
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| DOID:10652 | Alzheimer's disease | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
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| DOID:11832 | visual epilepsy | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
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| DOID:885 | fascioliasis | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
|
