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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:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:10825 | essential hypertension | HGNC:804 | Homo sapiens (human) | 481 | ATP1B1 |
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| DOID:0080226 | autosomal dominant intellectual developmental disorder 56 | HGNC:2092 | Homo sapiens (human) | 1213 | CLTC |
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| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
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| DOID:10584 | retinitis pigmentosa | HGNC:6055 | Homo sapiens (human) | 3617 | IMPG1 |
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| DOID:0080734 | Ehlers-Danlos syndrome kyphoscoliotic type 1 | HGNC:9081 | Homo sapiens (human) | 5351 | PLOD1 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:0080612 | anterior segment dysgenesis 7 | HGNC:14966 | Homo sapiens (human) | 7837 | PXDN |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:13841 | Homo sapiens (human) | 57211 | ADGRG6 |
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| DOID:0060765 | autosomal dominant Robinow syndrome 2 | HGNC:3084 | Homo sapiens (human) | 1855 | DVL1 |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | HGNC:923 | Homo sapiens (human) | 26229 | B3GAT3 |
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| DOID:13910 | red color blindness | HGNC:9936 | Homo sapiens (human) | 5956 | OPN1LW |
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| DOID:0110513 | autosomal recessive nonsyndromic deafness 61 | HGNC:9359 | Homo sapiens (human) | 375611 | SLC26A5 |
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| DOID:3070 | high grade glioma | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:0111979 | immunodeficiency 49 | HGNC:13222 | Homo sapiens (human) | 64919 | BCL11B |
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| DOID:0111444 | progressive myoclonus epilepsy 4 | HGNC:1665 | Homo sapiens (human) | 950 | SCARB2 |
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| DOID:0111447 | progressive myoclonus epilepsy 7 | HGNC:6233 | Homo sapiens (human) | 3746 | KCNC1 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:10534 | stomach cancer | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0060297 | complement component 4a deficiency | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:0112040 | non-syndromic X-linked intellectual disability 100 | HGNC:13339 | Homo sapiens (human) | 24137 | KIF4A |
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| DOID:0090070 | hypogonadotropic hypogonadism | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
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| DOID:0050858 | Marshall-Smith syndrome | HGNC:7788 | Homo sapiens (human) | 4784 | NFIX |
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| DOID:0111577 | dehydrated hereditary stomatocytosis 2 | HGNC:6293 | Homo sapiens (human) | 3783 | KCNN4 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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