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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:0050569 | Seckel syndrome | HGNC:33499 | Homo sapiens (human) | 84126 | ATRIP |
|
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| DOID:0060041 | autism spectrum disorder | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
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| DOID:0111169 | subcortical band heterotopia | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
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| DOID:0050453 | lissencephaly | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
|
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| DOID:1682 | congenital heart disease | HGNC:20068 | Homo sapiens (human) | 84132 | USP42 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:20068 | Homo sapiens (human) | 84132 | USP42 |
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| DOID:0110365 | retinitis pigmentosa 28 | HGNC:25808 | Homo sapiens (human) | 84140 | FAM161A |
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| DOID:11830 | myopia | HGNC:29222 | Homo sapiens (human) | 84146 | ZNF644 |
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| DOID:1612 | breast cancer | HGNC:17933 | Homo sapiens (human) | 84148 | KAT8 |
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| DOID:4467 | clear cell renal cell carcinoma | HGNC:17933 | Homo sapiens (human) | 84148 | KAT8 |
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| DOID:0111555 | Alkuraya-Kucinskas syndrome | HGNC:26953 | Homo sapiens (human) | 84162 | BLTP1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:29933 | Homo sapiens (human) | 84166 | NLRC5 |
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| DOID:0080199 | colorectal carcinoma | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
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| DOID:0060081 | triple-receptor negative breast cancer | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
|
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| DOID:4948 | gallbladder carcinoma | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
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| DOID:1612 | breast cancer | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
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| DOID:9256 | colorectal cancer | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
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| DOID:0112249 | GAPO syndrome | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
|
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| DOID:0080792 | Treacher Collins syndrome 4 | HGNC:20454 | Homo sapiens (human) | 84172 | POLR1B |
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| DOID:2908 | Treacher Collins syndrome | HGNC:20454 | Homo sapiens (human) | 84172 | POLR1B |
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| DOID:1682 | congenital heart disease | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:0060041 | autism spectrum disorder | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:0050834 | CHARGE syndrome | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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| DOID:0111628 | high myopia-sensorineural deafness syndrome | HGNC:23503 | Homo sapiens (human) | 84189 | SLITRK6 |
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