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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:14115 | toxic shock syndrome | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:4797 | SM-AHNMD | HGNC:18318 | Homo sapiens (human) | 171023 | ASXL1 |
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| DOID:1875 | impotence | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:1909 | melanoma | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:10907 | microcephaly | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:3525 | middle cerebral artery infarction | RGD:2493 | Rattus norvegicus (Norway rat) | 24310 | Ace |
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| DOID:594 | panic disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:6419 | tetralogy of Fallot | HGNC:33983 | Homo sapiens (human) | 653275 | CFC1B |
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| DOID:1059 | intellectual disability | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0080615 | nephroma | HGNC:17098 | Homo sapiens (human) | 23405 | DICER1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:4854 | Homo sapiens (human) | 8841 | HDAC3 |
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| DOID:1967 | leiomyosarcoma | HGNC:12836 | Homo sapiens (human) | 22803 | XRN2 |
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| DOID:13922 | eosinophilic esophagitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:5603 | T-cell acute lymphoblastic leukemia | HGNC:8803 | Homo sapiens (human) | 5156 | PDGFRA |
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| DOID:8692 | myeloid leukemia | HGNC:8803 | Homo sapiens (human) | 5156 | PDGFRA |
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| DOID:1389 | polyneuropathy | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:9281 | phenylketonuria | RGD:2645 | Rattus norvegicus (Norway rat) | 24377 | G6pd |
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| DOID:8893 | psoriasis | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:1612 | breast cancer | HGNC:15840 | Homo sapiens (human) | 9757 | KMT2B |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1358 | Homo sapiens (human) | 735 | C9 |
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| DOID:0080322 | polycystic kidney disease | RGD:620319 | Rattus norvegicus (Norway rat) | 117512 | C9 |
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