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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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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:1287 | cardiovascular system disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1074 | kidney failure | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1984 | rectal benign neoplasm | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0050589 | inflammatory bowel disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3069 | malignant astrocytoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:423 | myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9970 | obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:657 | adenoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:2747 | glycogen storage disease | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:0080191 | PTEN hamartoma tumor syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:9182 | pemphigus | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1508 | candidiasis | HGNC:4016 | Homo sapiens (human) | 2527 | FUT5 |
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| DOID:790 | ocular hypotension | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:5082 | liver cirrhosis | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:14330 | Parkinson's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:2316 | brain ischemia | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:10584 | retinitis pigmentosa | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:6000 | congestive heart failure | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:10763 | hypertension | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:0081292 | traumatic brain injury | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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