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GlyTouCan
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:1459 | hypothyroidism | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:11801 | protein-energy malnutrition | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9970 | obesity | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:326 | ischemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:3393 | coronary artery disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1184 | nephrotic syndrome | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:10763 | hypertension | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3393 | coronary artery disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:1287 | cardiovascular system disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:9970 | obesity | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3526 | cerebral infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:2211 | factor XIII deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:2216 | factor V deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:3413 | alpha-mannosidosis | FB:FBgn0027611 | Drosophila melanogaster (fruit fly) | 34437 | LManII | CG6206 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | Xenbase:XB-GENE-941057 | Xenopus laevis (African clawed frog) | 108715547 | LOC108715547 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | Xenbase:XB-GENE-941057 | Xenopus laevis (African clawed frog) | 108715547 | LOC108715547 |
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| DOID:3146 | lipid metabolism disorder | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:811 | lipodystrophy | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0080108 | myoglobinuria | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:11981 | morbid obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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