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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:3068 | glioblastoma | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:2383 | neonatal jaundice | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:2352 | hemochromatosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:557 | kidney disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:6713 | cerebrovascular disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:1074 | kidney failure | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:1686 | glaucoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:10652 | Alzheimer's disease | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:3070 | high grade glioma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:3070 | high grade glioma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:9970 | obesity | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:9279 | hyperhomocysteinemia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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