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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:1824 | status epilepticus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0014667 | disease of metabolism | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:2957 | pulmonary tuberculosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:8893 | psoriasis | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3513 | Homo sapiens (human) | 2132 | EXT2 |
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| DOID:9870 | galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:8029 | sporadic breast cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:1826 | epilepsy | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:161 | keratosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8505 | dermatitis herpetiformis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5742 | pancreatic acinar cell adenocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10534 | stomach cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9452 | steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:2316 | brain ischemia | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:1824 | status epilepticus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8973 | Homo sapiens (human) | 5288 | PIK3C2G |
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| DOID:9970 | obesity | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:1394 | urinary schistosomiasis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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