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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:0070398 | hypomyelinating leukodystrophy 15 | HGNC:3418 | Homo sapiens (human) | 2058 | EPRS1 |
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| DOID:0110063 | amelogenesis imperfecta hypomaturation type 2A5 | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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| DOID:0112038 | non-syndromic X-linked intellectual disability 1 | HGNC:29059 | Homo sapiens (human) | 23096 | IQSEC2 |
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| DOID:0111705 | oculoectodermal syndrome | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0060774 | congenital diarrhea | HGNC:12781 | Homo sapiens (human) | 7482 | WNT2B |
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| DOID:0070229 | intrahepatic cholestasis of pregnancy 3 | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0070204 | familial partial lipodystrophy type 3 | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:7004 | ACTH-secreting pituitary adenoma | HGNC:12631 | Homo sapiens (human) | 9101 | USP8 |
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| DOID:0060805 | Prieto syndrome | HGNC:14543 | Homo sapiens (human) | 65267 | WNK3 |
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| DOID:0080170 | normophosphatemic familial tumoral calcinosis | HGNC:1348 | Homo sapiens (human) | 54809 | SAMD9 |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0112277 | immunodeficiency 79 | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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| DOID:0080751 | keratosis pilaris atrophicans | HGNC:6692 | Homo sapiens (human) | 4035 | LRP1 |
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| DOID:9256 | colorectal cancer | HGNC:27310 | Homo sapiens (human) | 201163 | FLCN |
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| DOID:0110070 | arrhythmogenic right ventricular dysplasia 1 | HGNC:11769 | Homo sapiens (human) | 7043 | TGFB3 |
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| DOID:0111956 | immunodeficiency 27B | HGNC:5439 | Homo sapiens (human) | 3459 | IFNGR1 |
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| DOID:0111706 | oblique facial clefting 1 | HGNC:29022 | Homo sapiens (human) | 23384 | SPECC1L |
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| DOID:0050680 | Boomerang dysplasia | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0060295 | complement component 2 deficiency | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0090041 | torsion dystonia 4 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0070168 | spermatogenic failure 3 | HGNC:14468 | Homo sapiens (human) | 116369 | SLC26A8 |
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| DOID:0110838 | Usher syndrome type 2A | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:0060023 | immunodeficiency with hyper IgM type 3 | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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