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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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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:684 | hepatocellular carcinoma | HGNC:11724 | Homo sapiens (human) | 7010 | TEK |
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| DOID:6432 | pulmonary hypertension | HGNC:11724 | Homo sapiens (human) | 7010 | TEK |
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| DOID:3008 | invasive ductal carcinoma | HGNC:11723 | Homo sapiens (human) | 7009 | TMBIM6 |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:11723 | Homo sapiens (human) | 7009 | TMBIM6 |
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| DOID:10286 | prostate carcinoma | HGNC:11723 | Homo sapiens (human) | 7009 | TMBIM6 |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0112332 | pontocerebellar hypoplasia type 13 | HGNC:1172 | Homo sapiens (human) | 738 | VPS51 |
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| DOID:0111228 | Sveinsson chorioretinal atrophy | HGNC:11714 | Homo sapiens (human) | 7003 | TEAD1 |
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| DOID:12271 | aniridia | HGNC:1171 | Homo sapiens (human) | 26610 | ELP4 |
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| DOID:219 | colon cancer | HGNC:11701 | Homo sapiens (human) | 6997 | CRIPTO |
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| DOID:1682 | congenital heart disease | HGNC:11701 | Homo sapiens (human) | 6997 | CRIPTO |
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| DOID:0080074 | neural tube defect | HGNC:11701 | Homo sapiens (human) | 6997 | CRIPTO |
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| DOID:1724 | duodenal ulcer | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:2908 | Treacher Collins syndrome | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
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| DOID:0080789 | Treacher Collins syndrome 1 | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
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| DOID:1324 | lung cancer | HGNC:1165 | Homo sapiens (human) | 747 | DAGLA |
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| DOID:0050827 | rheumatic heart disease | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:9408 | acute myocardial infarction | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:0110857 | posterior polymorphous corneal dystrophy 3 | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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