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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:11650 | bronchopulmonary dysplasia | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6895 | Homo sapiens (human) | 8685 | MARCO |
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| DOID:718 | autoimmune hemolytic anemia | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:1993 | rectum cancer | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:2569 | retinal drusen | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1229 | paranoid schizophrenia | HGNC:6292 | Homo sapiens (human) | 3782 | KCNN3 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:7516 | Homo sapiens (human) | 727897 | MUC5B |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:0060686 | autosomal dominant nocturnal frontal lobe epilepsy 5 | HGNC:18865 | Homo sapiens (human) | 57582 | KCNT1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:1793 | pancreatic cancer | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:1790 | malignant mesothelioma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:3883 | Lynch syndrome | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:0070478 | diphthamide deficiency syndrome 2 | HGNC:3004 | Homo sapiens (human) | 1802 | DPH2 |
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| DOID:13580 | cholestasis | HGNC:1983 | Homo sapiens (human) | 84916 | UTP4 |
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| DOID:9970 | obesity | HGNC:5295 | Homo sapiens (human) | 3358 | HTR2C |
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| DOID:1324 | lung cancer | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:14498 | lipoid proteinosis | HGNC:3153 | Homo sapiens (human) | 1893 | ECM1 |
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| DOID:83 | cataract | HGNC:7782 | Homo sapiens (human) | 4780 | NFE2L2 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:22197 | Homo sapiens (human) | 9907 | AP5Z1 |
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| DOID:0111526 | Mullerian aplasia and hyperandrogenism | HGNC:12783 | Homo sapiens (human) | 54361 | WNT4 |
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| DOID:0111556 | steatocystoma multiplex | HGNC:6427 | Homo sapiens (human) | 3872 | KRT17 |
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