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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: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:0111446 | progressive myoclonus epilepsy 3 | SGD:S000005569 | Saccharomyces cerevisiae S288C | 854208 | WHI2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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| DOID:0110840 | Usher syndrome type 2D | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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| DOID:0110490 | autosomal recessive nonsyndromic deafness 31 | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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| DOID:1612 | breast cancer | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:10283 | prostate cancer | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:11054 | urinary bladder cancer | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:2154 | nephroblastoma | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:0050685 | small cell carcinoma | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:4450 | renal cell carcinoma | HGNC:18081 | Homo sapiens (human) | 11197 | WIF1 |
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| DOID:12858 | Huntington's disease | HGNC:25471 | Homo sapiens (human) | 55062 | WIPI1 |
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| DOID:12858 | Huntington's disease | HGNC:32225 | Homo sapiens (human) | 26100 | WIPI2 |
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| DOID:1936 | atherosclerosis | HGNC:30917 | Homo sapiens (human) | 58525 | WIZ |
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| DOID:0070473 | Zaki syndrome | HGNC:30238 | Homo sapiens (human) | 79971 | WLS |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:224 | transient cerebral ischemia | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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