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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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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:0050650 | familial atrial fibrillation | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0110222 | Brugada syndrome 5 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0080455 | developmental and epileptic encephalopathy 52 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0080422 | Dravet syndrome | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:1826 | epilepsy | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:2030 | anxiety disorder | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0060041 | autism spectrum disorder | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0111183 | familial hemiplegic migraine 3 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0070379 | developmental and epileptic encephalopathy 6B | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:2018 | hyperinsulinism | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:397 | restrictive cardiomyopathy | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:305 | carcinoma | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:0050958 | spinocerebellar ataxia type 7 | HGNC:10560 | Homo sapiens (human) | 6314 | ATXN7 |
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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: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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