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GlyTouCan
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
LM-GlycoRepo
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:5844 | myocardial infarction | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:11981 | morbid obesity | HGNC:15879 | Homo sapiens (human) | 56259 | CTNNBL1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:5033 | Homo sapiens (human) | 3181 | HNRNPA2B1 |
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| DOID:986 | alopecia areata | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10534 | stomach cancer | HGNC:6019 | Homo sapiens (human) | 3570 | IL6R |
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| DOID:1070 | primary open angle glaucoma | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0080959 | arrhythmogenic right ventricular dysplasia 14 | HGNC:1759 | Homo sapiens (human) | 1000 | CDH2 |
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| DOID:0060574 | von Willebrand's disease 2 | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0111699 | Van den Ende-Gupta syndrome | HGNC:19869 | Homo sapiens (human) | 91179 | SCARF2 |
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| DOID:12804 | mucopolysaccharidosis IV | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080329 | cold-induced sweating syndrome 1 | HGNC:2364 | Homo sapiens (human) | 9244 | CRLF1 |
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| DOID:0050942 | spastic ataxia 3 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:0111363 | Heinz body anemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0110536 | autosomal recessive nonsyndromic deafness 91 | HGNC:8950 | Homo sapiens (human) | 5269 | SERPINB6 |
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| DOID:12306 | vitiligo | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:9827 | radioulnar synostosis | HGNC:5101 | Homo sapiens (human) | 3207 | HOXA11 |
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| DOID:0080545 | hyper IgE syndrome | HGNC:6019 | Homo sapiens (human) | 3570 | IL6R |
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| DOID:1470 | major depressive disorder | HGNC:7978 | Homo sapiens (human) | 2908 | NR3C1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:783 | end stage renal disease | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:0080940 | hereditary angioedema type III | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:1019 | osteomyelitis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0081343 | congenital myopathy 9A | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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| DOID:4450 | renal cell carcinoma | HGNC:11752 | Homo sapiens (human) | 7030 | TFE3 |
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