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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:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:0050773 | paraganglioma | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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| DOID:0080110 | contractures, pterygia, and spondylocarpotarsal fusion syndrome | HGNC:1967 | Homo sapiens (human) | 1146 | CHRNG |
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| DOID:0060733 | junctional epidermolysis bullosa with pyloric atresia | HGNC:6142 | Homo sapiens (human) | 3655 | ITGA6 |
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| DOID:0110160 | Charcot-Marie-Tooth disease axonal type 2T | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:0110200 | Charcot-Marie-Tooth disease dominant intermediate D | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:29955 | Homo sapiens (human) | 200931 | SLC51A |
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| DOID:0112121 | nephrogenic syndrome of inappropriate antidiuresis | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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| DOID:0081230 | autosomal recessive intellectual developmental disorder 69 | HGNC:16740 | Homo sapiens (human) | 27107 | ZBTB11 |
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| DOID:0081153 | common variable immunodeficiency 11 | HGNC:6005 | Homo sapiens (human) | 59067 | IL21 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:8063 | Homo sapiens (human) | 9631 | NUP155 |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:4239 | alveolar soft part sarcoma | HGNC:13825 | Homo sapiens (human) | 79058 | ASPSCR1 |
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| DOID:0080549 | Noonan syndrome with multiple lentigines 2 | HGNC:9829 | Homo sapiens (human) | 5894 | RAF1 |
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| DOID:0081141 | agammaglobulinemia 9 | HGNC:4927 | Homo sapiens (human) | 7922 | SLC39A7 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:0111111 | maturity-onset diabetes of the young type 14 | HGNC:24035 | Homo sapiens (human) | 26060 | APPL1 |
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| DOID:10825 | essential hypertension | HGNC:3146 | Homo sapiens (human) | 1889 | ECE1 |
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| DOID:0080675 | Stickler syndrome 2 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0060883 | intestinal hypomagnesemia 1 | HGNC:17995 | Homo sapiens (human) | 140803 | TRPM6 |
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| DOID:0080551 | Naxos disease | HGNC:6207 | Homo sapiens (human) | 3728 | JUP |
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