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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:633 | myositis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0081369 | Paget's disease of bone 6 | HGNC:29277 | Homo sapiens (human) | 57592 | ZNF687 |
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| DOID:9976 | heroin dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:0080188 | chronic myelomonocytic leukemia | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:5041 | esophageal cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:988 | mitral valve prolapse | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0110389 | retinitis pigmentosa 73 | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:13918 | Homo sapiens (human) | 7916 | PRRC2A |
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| DOID:2043 | hepatitis B | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:0111405 | Fraser syndrome 1 | HGNC:19185 | Homo sapiens (human) | 80144 | FRAS1 |
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| DOID:0110770 | hereditary spastic paraplegia 17 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:850 | lung disease | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:1485 | cystic fibrosis | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0080420 | developmental and epileptic encephalopathy 62 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0112353 | spermatogenic failure 64 | HGNC:28521 | Homo sapiens (human) | 286151 | FBXO43 |
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| DOID:0080957 | primary hypoalphalipoproteinemia 1 | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
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| DOID:557 | kidney disease | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0111398 | congenital dyserythropoietic anemia type Ia | HGNC:1713 | Homo sapiens (human) | 146059 | CDAN1 |
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| DOID:1612 | breast cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1380 | endometrial cancer | HGNC:6190 | Homo sapiens (human) | 3716 | JAK1 |
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| DOID:0112145 | retinitis pigmentosa 88 | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:3526 | cerebral infarction | HGNC:5434 | Homo sapiens (human) | 3456 | IFNB1 |
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| DOID:1324 | lung cancer | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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