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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:0060072 | benign neoplasm | HGNC:6514 | Homo sapiens (human) | 9113 | LATS1 |
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| DOID:1289 | neurodegenerative disease | HGNC:6514 | Homo sapiens (human) | 9113 | LATS1 |
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| DOID:1319 | brain cancer | HGNC:26677 | Homo sapiens (human) | 91133 | L3MBTL4 |
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| DOID:10908 | hydrocephalus | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:576 | proteinuria | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:10762 | portal hypertension | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:12712 | nephronophthisis | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0050778 | Meckel syndrome | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:2975 | cystic kidney disease | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0111589 | COACH syndrome | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0111001 | Joubert syndrome 6 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0050545 | visceral heterotaxy | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0110136 | Bardet-Biedl syndrome 14 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0060340 | ciliopathy | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0070117 | Meckel syndrome 3 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0111118 | nephronophthisis 11 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:1088 | meningocele | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:12270 | coloboma | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:1573 | communicating hydrocephalus | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0111699 | Van den Ende-Gupta syndrome | HGNC:19869 | Homo sapiens (human) | 91179 | SCARF2 |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:10534 | stomach cancer | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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