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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:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:11054 | urinary bladder cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:162 | cancer | HGNC:9283 | Homo sapiens (human) | 5501 | PPP1CC |
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| DOID:820 | myocarditis | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:9974 | drug dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:6432 | pulmonary hypertension | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0050827 | rheumatic heart disease | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:10591 | pre-eclampsia | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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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:4450 | renal cell carcinoma | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:4752 | multiple system atrophy | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:11446 | sciatic neuropathy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:3146 | lipid metabolism disorder | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:3459 | breast carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:3393 | coronary artery disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:11476 | osteoporosis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050771 | pheochromocytoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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