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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:13580 | cholestasis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:4362 | cervical cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:341 | peripheral vascular disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2531 | hematologic cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3021 | acute kidney failure | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0081023 | retinal cone dystrophy 4 | HGNC:20202 | Homo sapiens (human) | 93589 | CACNA2D4 |
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| DOID:8466 | retinal degeneration | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:224 | transient cerebral ischemia | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:3891 | placental insufficiency | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0060496 | respiratory allergy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:2987 | familial mediterranean fever | HGNC:2637 | Homo sapiens (human) | 1576 | CYP3A4 |
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| DOID:0050883 | infantile cerebellar-retinal degeneration | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:14221 | abdominal obesity-metabolic syndrome 1 | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:684 | hepatocellular carcinoma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:850 | lung disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1059 | intellectual disability | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:9256 | colorectal cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:0050741 | alcohol dependence | HGNC:252 | Homo sapiens (human) | 127 | ADH4 |
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| DOID:784 | chronic kidney disease | HGNC:1548 | Homo sapiens (human) | 873 | CBR1 |
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