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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:10159 | osteonecrosis | HGNC:537 | Homo sapiens (human) | 302 | ANXA2 |
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| DOID:0070121 | Meckel syndrome 7 | HGNC:7907 | Homo sapiens (human) | 27031 | NPHP3 |
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| DOID:0050742 | nicotine dependence | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:5419 | schizophrenia | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:2957 | pulmonary tuberculosis | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:11054 | urinary bladder cancer | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:10763 | hypertension | HGNC:4464 | Homo sapiens (human) | 2834 | PRLHR |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:23631 | Homo sapiens (human) | 387129 | NPSR1 |
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| DOID:9993 | hypoglycemia | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:8923 | skin melanoma | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:10763 | hypertension | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0110987 | Joubert syndrome 18 | HGNC:24519 | Homo sapiens (human) | 26123 | TCTN3 |
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| DOID:5688 | Werner syndrome | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:936 | brain disease | HGNC:15594 | Homo sapiens (human) | 51163 | DBR1 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:3492 | mixed connective tissue disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111818 | syndactyly type 4 | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0111583 | carboxypeptidase N deficiency | HGNC:2312 | Homo sapiens (human) | 1369 | CPN1 |
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| DOID:0111399 | congenital dyserythropoietic anemia type III | HGNC:6392 | Homo sapiens (human) | 9493 | KIF23 |
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| DOID:0080820 | occupational asthma | HGNC:4962 | Homo sapiens (human) | 3133 | HLA-E |
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| DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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