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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:0050564 | autosomal dominant nonsyndromic deafness | HGNC:18533 | Homo sapiens (human) | 84196 | USP48 |
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| DOID:0070062 | Arboleda-Tham syndrome | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:9620 | vesicoureteral reflux | HGNC:11976 | Homo sapiens (human) | 7148 | TNXB |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:2280 | hidradenitis suppurativa | HGNC:17091 | Homo sapiens (human) | 23385 | NCSTN |
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| DOID:0080716 | infantile liver failure syndrome | HGNC:15625 | Homo sapiens (human) | 51594 | NBAS |
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| DOID:2436 | glomangioma | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:1588 | thrombocytopenia | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0112192 | tetraamelia syndrome 1 | HGNC:12782 | Homo sapiens (human) | 7473 | WNT3 |
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| DOID:0090135 | complex cortical dysplasia with other brain malformations 5 | HGNC:12412 | Homo sapiens (human) | 7280 | TUBB2A |
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| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
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| DOID:10908 | hydrocephalus | HGNC:7208 | Homo sapiens (human) | 8777 | MPDZ |
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| DOID:12849 | autistic disorder | HGNC:14295 | Homo sapiens (human) | 22941 | SHANK2 |
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| DOID:0060222 | Scheie syndrome | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0110566 | autosomal dominant nonsyndromic deafness 40 | HGNC:2418 | Homo sapiens (human) | 1428 | CRYM |
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| DOID:0050470 | Donohue syndrome | HGNC:6091 | Homo sapiens (human) | 3643 | INSR |
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| DOID:0050741 | alcohol dependence | HGNC:14921 | Homo sapiens (human) | 50833 | TAS2R16 |
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| DOID:12365 | malaria | HGNC:7873 | Homo sapiens (human) | 4843 | NOS2 |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:0110174 | Charcot-Marie-Tooth disease axonal type 2L | HGNC:30171 | Homo sapiens (human) | 26353 | HSPB8 |
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| DOID:0080315 | megalencephalic leukoencephalopathy with subcortical cysts | HGNC:13308 | Homo sapiens (human) | 51704 | GPRC5B |
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| DOID:0080284 | developmental and epileptic encephalopathy 57 | HGNC:18866 | Homo sapiens (human) | 343450 | KCNT2 |
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| DOID:0070484 | Legius syndrome | HGNC:20249 | Homo sapiens (human) | 161742 | SPRED1 |
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| DOID:0080837 | growth hormone insensitivity syndrome with immune dysregulation 2 | HGNC:11367 | Homo sapiens (human) | 6777 | STAT5B |
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