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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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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:5844 | myocardial infarction | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:783 | end stage renal disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:1586 | rheumatic fever | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:11054 | urinary bladder cancer | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:614 | lymphopenia | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0060573 | von Willebrand's disease 1 | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:0111634 | autosomal recessive nonsyndromic deafness 99 | HGNC:26991 | Homo sapiens (human) | 124842 | TMEM132E |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:7979 | Homo sapiens (human) | 4306 | NR3C2 |
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| DOID:2272 | vulvovaginal candidiasis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1324 | lung cancer | HGNC:3087 | Homo sapiens (human) | 1857 | DVL3 |
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| DOID:0060772 | multiple types of congenital heart defects 6 | HGNC:4214 | Homo sapiens (human) | 2657 | GDF1 |
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| DOID:234 | colon adenocarcinoma | RGD:70487 | Rattus norvegicus (Norway rat) | 84353 | Ctnnb1 |
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| DOID:0112228 | lissencephaly 9 with complex brainstem malformation | HGNC:13664 | Homo sapiens (human) | 23499 | MACF1 |
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| DOID:2987 | familial mediterranean fever | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:6419 | tetralogy of Fallot | HGNC:6188 | Homo sapiens (human) | 182 | JAG1 |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:13141 | uveitis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:1580 | diffuse scleroderma | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:1936 | atherosclerosis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:576 | proteinuria | RGD:620100 | Rattus norvegicus (Norway rat) | 65271 | Mgat5 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12665 | Homo sapiens (human) | 7414 | VCL |
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| DOID:0110654 | long QT syndrome 13 | HGNC:6266 | Homo sapiens (human) | 3762 | KCNJ5 |
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| DOID:0111467 | combined oxidative phosphorylation deficiency 13 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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