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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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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:7147 | ankylosing spondylitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1574 | alcohol use disorder | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:9970 | obesity | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:12306 | vitiligo | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:10579 | leukodystrophy | HGNC:16066 | Homo sapiens (human) | 55331 | ACER3 |
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| DOID:1459 | hypothyroidism | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2797 | idiopathic interstitial pneumonia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0050860 | colorectal adenoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:2316 | brain ischemia | HGNC:9035 | Homo sapiens (human) | 5321 | PLA2G4A |
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| DOID:3454 | brain infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:0060076 | estrogen-receptor negative breast cancer | HGNC:2873 | Homo sapiens (human) | 1727 | CYB5R3 |
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| DOID:10591 | pre-eclampsia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:10609 | rickets | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:11832 | visual epilepsy | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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