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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:0111739 | X-linked deafness 1 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0050432 | Asperger syndrome | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:9884 | muscular dystrophy | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:9974 | drug dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:2355 | anemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:3393 | coronary artery disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:10652 | Alzheimer's disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:3310 | atopic dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:3121 | gallbladder cancer | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:1574 | alcohol use disorder | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:1115 | sarcoma | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:1067 | open-angle glaucoma | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:11963 | esophagitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080520 | Tn polyagglutination syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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