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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:0070056 | autosomal dominant intellectual developmental disorder 26 | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:10907 | microcephaly | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:1574 | alcohol use disorder | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:1319 | brain cancer | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:2871 | endometrial carcinoma | HGNC:11390 | Homo sapiens (human) | 9212 | AURKB |
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| DOID:0050958 | spinocerebellar ataxia type 7 | HGNC:22210 | Homo sapiens (human) | 222255 | ATXN7L1 |
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| DOID:0050958 | spinocerebellar ataxia type 7 | HGNC:10560 | Homo sapiens (human) | 6314 | ATXN7 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:7106 | Homo sapiens (human) | 4287 | ATXN3 |
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| DOID:1440 | Machado-Joseph disease | HGNC:7106 | Homo sapiens (human) | 4287 | ATXN3 |
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| DOID:0050955 | spinocerebellar ataxia type 2 | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:0050955 | spinocerebellar ataxia type 2 | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:33279 | Homo sapiens (human) | 342371 | ATXN1L |
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| DOID:0050954 | spinocerebellar ataxia type 1 | HGNC:10548 | Homo sapiens (human) | 6310 | ATXN1 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:10548 | Homo sapiens (human) | 6310 | ATXN1 |
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| DOID:5409 | lung small cell carcinoma | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:1059 | intellectual disability | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:1115 | sarcoma | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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