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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:9952 | acute lymphoblastic leukemia | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:12306 | vitiligo | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:12849 | autistic disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0080429 | developmental and epileptic encephalopathy 24 | HGNC:4845 | Homo sapiens (human) | 348980 | HCN1 |
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| DOID:3082 | interstitial lung disease | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:1727 | retinal vein occlusion | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:9970 | obesity | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0110383 | retinitis pigmentosa 7 | HGNC:10254 | Homo sapiens (human) | 6094 | ROM1 |
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| DOID:0110057 | amelogenesis imperfecta type 2A1 | HGNC:6365 | Homo sapiens (human) | 9622 | KLK4 |
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| DOID:10534 | stomach cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:418 | systemic scleroderma | HGNC:7884 | Homo sapiens (human) | 4855 | NOTCH4 |
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| DOID:0111474 | combined oxidative phosphorylation deficiency 1 | HGNC:13780 | Homo sapiens (human) | 85476 | GFM1 |
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| DOID:0110648 | long QT syndrome 6 | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | HGNC:10256 | Homo sapiens (human) | 4919 | ROR1 |
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| DOID:980 | choroidal sclerosis | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:12930 | dilated cardiomyopathy | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:4362 | cervical cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0050857 | Perrault syndrome | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:13241 | Behcet's disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:0080893 | Bainbridge-Ropers syndrome | HGNC:29357 | Homo sapiens (human) | 80816 | ASXL3 |
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| DOID:0110876 | holoprosencephaly 7 | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:1657 | ventricular septal defect | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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