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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:14004 | thoracic aortic aneurysm | HGNC:9414 | Homo sapiens (human) | 5592 | PRKG1 |
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| DOID:0080413 | developmental and epileptic encephalopathy 18 | HGNC:29040 | Homo sapiens (human) | 23334 | SZT2 |
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| DOID:1380 | endometrial cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:12449 | aplastic anemia | HGNC:9360 | Homo sapiens (human) | 5551 | PRF1 |
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| DOID:0050986 | spinocerebellar ataxia type 40 | HGNC:19967 | Homo sapiens (human) | 440193 | CCDC88C |
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| DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:0110994 | Joubert syndrome 25 | HGNC:24866 | Homo sapiens (human) | 9731 | CEP104 |
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| DOID:0080502 | GM1 gangliosidosis type 1 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080939 | hereditary angioedema type I | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:6846 | familial melanoma | HGNC:7105 | Homo sapiens (human) | 4286 | MITF |
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| DOID:0060278 | pontocerebellar hypoplasia type 9 | HGNC:469 | Homo sapiens (human) | 271 | AMPD2 |
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| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:29619 | Homo sapiens (human) | 219972 | MPEG1 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0090094 | hypogonadotropic hypogonadism 1 with or without anosmia | HGNC:6211 | Homo sapiens (human) | 3730 | ANOS1 |
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| DOID:0111133 | focal segmental glomerulosclerosis 8 | HGNC:14082 | Homo sapiens (human) | 54443 | ANLN |
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| DOID:0112194 | Filippi syndrome | HGNC:26877 | Homo sapiens (human) | 150468 | CKAP2L |
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| DOID:0111561 | stiff skin syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:7608 | Homo sapiens (human) | 4649 | MYO9A |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:4997 | Camurati-Engelmann disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0080431 | developmental and epileptic encephalopathy 19 | HGNC:4075 | Homo sapiens (human) | 2554 | GABRA1 |
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| DOID:0110064 | amelogenesis imperfecta type 1H | HGNC:6161 | Homo sapiens (human) | 3694 | ITGB6 |
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