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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:9970 | obesity | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:9884 | muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:783 | end stage renal disease | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:9008 | psoriatic arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:13088 | periventricular leukomalacia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9256 | colorectal cancer | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:9256 | colorectal cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:2349 | arteriosclerosis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:3407 | carotid artery disease | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:12798 | mucopolysaccharidosis | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:10591 | pre-eclampsia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:5844 | myocardial infarction | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:4079 | heart valve disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8893 | psoriasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:9970 | obesity | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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