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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:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:4483 | rhinitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:4362 | cervical cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:4125 | Homo sapiens (human) | 2591 | GALNT3 |
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| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:783 | end stage renal disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:783 | end stage renal disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0050589 | inflammatory bowel disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:3393 | coronary artery disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0050474 | Netherton syndrome | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:10763 | hypertension | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:2747 | glycogen storage disease | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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| DOID:1056 | oculocerebrorenal syndrome | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:9970 | obesity | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:3312 | bipolar disorder | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:10754 | otitis media | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:1612 | breast cancer | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:12306 | vitiligo | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060041 | autism spectrum disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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