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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:8991 | cervix uteri carcinoma in situ | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111166 | molybdenum cofactor deficiency type C | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0080376 | trichorhinophalangeal syndrome type III | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:302 | substance abuse | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | HGNC:32456 | Homo sapiens (human) | 440138 | ALG11 |
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| DOID:3393 | coronary artery disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:11830 | myopia | HGNC:8547 | Homo sapiens (human) | 8974 | P4HA2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:986 | alopecia areata | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:10907 | microcephaly | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:3393 | coronary artery disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080839 | X-linked warfarin sensitivity | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0111086 | Fanconi anemia complementation group G | HGNC:3588 | Homo sapiens (human) | 2189 | FANCG |
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| DOID:4481 | allergic rhinitis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:12678 | hypercalcemia | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:19987 | Homo sapiens (human) | 284656 | EPHA10 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:2986 | IgA glomerulonephritis | HGNC:6027 | Homo sapiens (human) | 3579 | CXCR2 |
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