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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:0111315 | idiopathic generalized epilepsy 14 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:0060773 | cleft lip-palate-ectodermal dysplasia syndrome | HGNC:9706 | Homo sapiens (human) | 5818 | NECTIN1 |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080687 | reducing body myopathy 1B | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:0070480 | schwannomatosis 1 | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:25118 | Homo sapiens (human) | 90268 | OTULIN |
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| DOID:0110683 | congenital myasthenic syndrome 18 | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:0080385 | nephrotic syndrome type 11 | HGNC:29914 | Homo sapiens (human) | 57122 | NUP107 |
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| DOID:0110645 | long QT syndrome 2 | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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| DOID:0081368 | Paget's disease of bone 5 | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:7148 | rheumatoid arthritis | HGNC:10968 | Homo sapiens (human) | 6583 | SLC22A4 |
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| DOID:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0112281 | spondyloepiphyseal dysplasia Stanescu type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:4450 | renal cell carcinoma | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0110355 | retinitis pigmentosa 32 | HGNC:29675 | Homo sapiens (human) | 23155 | CLCC1 |
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| DOID:1682 | congenital heart disease | HGNC:17111 | Homo sapiens (human) | 171019 | ADAMTS19 |
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| DOID:0080105 | microcephaly and chorioretinopathy 1 | HGNC:18127 | Homo sapiens (human) | 85378 | TUBGCP6 |
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| DOID:0080328 | Culler-Jones syndrome | HGNC:4318 | Homo sapiens (human) | 2736 | GLI2 |
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| DOID:0080946 | retinal dystrophy with leukodystrophy | HGNC:23338 | Homo sapiens (human) | 91452 | ACBD5 |
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| DOID:0060366 | Hennekam syndrome | HGNC:219 | Homo sapiens (human) | 9508 | ADAMTS3 |
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| DOID:0060901 | lymphoplasmacytic lymphoma | HGNC:7562 | Homo sapiens (human) | 4615 | MYD88 |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:11813 | Homo sapiens (human) | 8914 | TIMELESS |
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| DOID:0111648 | ectopia lentis with ectopia of pupil | HGNC:19706 | Homo sapiens (human) | 54507 | ADAMTSL4 |
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| DOID:0110925 | familial hemophagocytic lymphohistiocytosis 5 | HGNC:11445 | Homo sapiens (human) | 6813 | STXBP2 |
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