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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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MIRAGE
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:2841 | asthma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:20474 | Homo sapiens (human) | 147138 | TMC8 |
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| DOID:0111305 | familial febrile seizures 4 | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:11563 | retinal vasculitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0111463 | cardiofaciocutaneous syndrome 4 | HGNC:6842 | Homo sapiens (human) | 5605 | MAP2K2 |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2256 | osteochondrodysplasia | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:0081236 | autosomal recessive intellectual developmental disorder 77 | HGNC:24866 | Homo sapiens (human) | 9731 | CEP104 |
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| DOID:14330 | Parkinson's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:2841 | asthma | HGNC:7512 | Homo sapiens (human) | 4583 | MUC2 |
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| DOID:1380 | endometrial cancer | HGNC:10839 | Homo sapiens (human) | 6462 | SHBG |
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| DOID:7148 | rheumatoid arthritis | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:3312 | bipolar disorder | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:10123 | pigmentation disease | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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| DOID:1555 | urticaria | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:0081371 | lacrimoauriculodentodigital syndrome 2 | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:5041 | esophageal cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0080376 | trichorhinophalangeal syndrome type III | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:670 | amphetamine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:2582 | acatalasia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:9669 | senile cataract | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:219 | colon cancer | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:12306 | vitiligo | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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