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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:0060674 | catecholaminergic polymorphic ventricular tachycardia | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:9975 | cocaine dependence | HGNC:1957 | Homo sapiens (human) | 1136 | CHRNA3 |
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| DOID:0060326 | myelomeningocele | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:10283 | prostate cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:1324 | lung cancer | HGNC:1165 | Homo sapiens (human) | 747 | DAGLA |
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| DOID:11832 | visual epilepsy | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0080594 | hyper IgE recurrent infection syndrome 2 | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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| DOID:612 | primary immunodeficiency disease | HGNC:9954 | Homo sapiens (human) | 5966 | REL |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:11714 | gestational diabetes | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0080763 | diffuse gastric cancer | HGNC:6848 | Homo sapiens (human) | 4214 | MAP3K1 |
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| DOID:13270 | erythropoietic protoporphyria | HGNC:2088 | Homo sapiens (human) | 10845 | CLPX |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:8766 | Homo sapiens (human) | 10015 | PDCD6IP |
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| DOID:0050778 | Meckel syndrome | HGNC:20652 | Homo sapiens (human) | 79770 | TXNDC15 |
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| DOID:0070279 | primary autosomal recessive microcephaly 14 | HGNC:25403 | Homo sapiens (human) | 163786 | SASS6 |
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| DOID:0070345 | vertebral anomalies and variable endocrine and T-cell dysfunction | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0111842 | Keipert syndrome | HGNC:4452 | Homo sapiens (human) | 2239 | GPC4 |
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| DOID:1070 | primary open angle glaucoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0110709 | hypotrichosis 12 | HGNC:10313 | Homo sapiens (human) | 6144 | RPL21 |
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| DOID:0080788 | proximal symphalangism 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0081263 | neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities | HGNC:15717 | Homo sapiens (human) | 50628 | GEMIN4 |
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| DOID:10159 | osteonecrosis | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:5679 | retinal disease | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:6254 | Homo sapiens (human) | 27133 | KCNH5 |
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