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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050460 | Wolf-Hirschhorn syndrome | HGNC:12766 | Homo sapiens (human) | 7468 | NSD2 |
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| DOID:225 | syndrome | HGNC:12766 | Homo sapiens (human) | 7468 | NSD2 |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:12766 | Homo sapiens (human) | 7468 | NSD2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:12766 | Homo sapiens (human) | 7468 | NSD2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:11832 | visual epilepsy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10603 | glucose intolerance | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:5723 | optic atrophy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:83 | cataract | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110241 | cataract 41 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2055 | post-traumatic stress disorder | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9351 | diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110629 | Wolfram syndrome 1 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:8947 | diabetic retinopathy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0111441 | optic atrophy 1 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0080584 | autosomal dominant Wolfram syndrome | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10632 | Wolfram syndrome | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:12760 | Homo sapiens (human) | 54014 | BRWD1 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:12755 | Homo sapiens (human) | 10885 | WDR3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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