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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:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
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| DOID:5723 | optic atrophy | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:9256 | colorectal cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0080596 | hyper IgE recurrent infection syndrome 4 | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | HGNC:28596 | Homo sapiens (human) | 148789 | B3GALNT2 |
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| DOID:0080502 | GM1 gangliosidosis type 1 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0111389 | mucopolysaccharidosis Ih/s | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4456 | Homo sapiens (human) | 2820 | GPD2 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
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| DOID:2582 | acatalasia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:9870 | galactosemia | HGNC:24063 | Homo sapiens (human) | 130589 | GALM |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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| DOID:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:0080952 | AMED syndrome | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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