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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:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:1742 | drug psychosis | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:10763 | hypertension | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:5419 | schizophrenia | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:684 | hepatocellular carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3320 | Tay-Sachs disease | HGNC:4878 | Homo sapiens (human) | 3073 | HEXA |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:9269 | maple syrup urine disease | HGNC:987 | Homo sapiens (human) | 594 | BCKDHB |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:13482 | Proteus syndrome | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:14330 | Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0050461 | aspartylglucosaminuria | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0050574 | L-2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:684 | hepatocellular carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:10591 | pre-eclampsia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050848 | obstructive sleep apnea | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:8947 | diabetic retinopathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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