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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:5381 | bile duct adenoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:0050884 | triosephosphate isomerase deficiency | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0110915 | childhood hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:0111254 | glutaric acidemia I | HGNC:4189 | Homo sapiens (human) | 2639 | GCDH |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:3413 | alpha-mannosidosis | HGNC:6826 | Homo sapiens (human) | 4125 | MAN2B1 |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:12799 | mucopolysaccharidosis II | HGNC:5389 | Homo sapiens (human) | 3423 | IDS |
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| DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:850 | lung disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0050773 | paraganglioma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:12798 | mucopolysaccharidosis | HGNC:25239 | Homo sapiens (human) | 153642 | ARSK |
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| DOID:14500 | fucosidosis | HGNC:4006 | Homo sapiens (human) | 2517 | FUCA1 |
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