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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:12678 | hypercalcemia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:50 | thyroid gland disease | HGNC:30972 | Homo sapiens (human) | 79048 | SECISBP2 |
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| DOID:12365 | malaria | HGNC:4703 | Homo sapiens (human) | 2994 | GYPB |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112346 | hereditary spastic paraplegia 83 | HGNC:28242 | Homo sapiens (human) | 84842 | HPDL |
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| DOID:0080686 | tubular aggregate myopathy 2 | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:2729 | dyskeratosis congenita | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:612 | primary immunodeficiency disease | HGNC:29418 | Homo sapiens (human) | 96459 | FNIP1 |
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| DOID:0080086 | nonsyndromic congenital nail disorder 8 | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0112334 | pontocerebellar hypoplasia type 1C | HGNC:17035 | Homo sapiens (human) | 11340 | EXOSC8 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6158 | Homo sapiens (human) | 3691 | ITGB4 |
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| DOID:0111424 | branchiootorenal syndrome 2 | HGNC:10891 | Homo sapiens (human) | 147912 | SIX5 |
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| DOID:0110672 | congenital myasthenic syndrome 21 | HGNC:10936 | Homo sapiens (human) | 6572 | SLC18A3 |
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| DOID:12849 | autistic disorder | HGNC:14291 | Homo sapiens (human) | 22871 | NLGN1 |
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| DOID:0110649 | long QT syndrome 8 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0110450 | dilated cardiomyopathy 1II | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:5374 | pilomatrixoma | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:9827 | radioulnar synostosis | HGNC:6772 | Homo sapiens (human) | 4091 | SMAD6 |
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| DOID:0111162 | epidermal nevus | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0110110 | atrial heart septal defect 5 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12949 | Homo sapiens (human) | 7716 | VEZF1 |
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| DOID:0111982 | immunodeficiency 56 | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:0090070 | hypogonadotropic hypogonadism | HGNC:26256 | Homo sapiens (human) | 79625 | NDNF |
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