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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
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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:874 | bacterial pneumonia | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:10534 | stomach cancer | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:1826 | epilepsy | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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| DOID:12894 | Sjogren's syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8725 | vascular dementia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10241 | thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9408 | acute myocardial infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080750 | erythema nodosum | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9588 | encephalitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8283 | peritonitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9008 | psoriatic arthritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1407 | anterior uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1227 | neutropenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050589 | inflammatory bowel disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12306 | vitiligo | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8505 | dermatitis herpetiformis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
