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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:3069 | malignant astrocytoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:10763 | hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:2560 | morphine dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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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: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: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: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:684 | hepatocellular carcinoma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0050741 | alcohol dependence | HGNC:252 | Homo sapiens (human) | 127 | ADH4 |
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| DOID:3393 | coronary artery disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
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| DOID:234 | colon adenocarcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:178 | vascular disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
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| DOID:2154 | nephroblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:9976 | heroin dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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