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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:10325 | silicosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:10763 | hypertension | HGNC:17423 | Homo sapiens (human) | 55501 | CHST12 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:17223 | Homo sapiens (human) | 10090 | UST |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:674 | cleft palate | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:1184 | nephrotic syndrome | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:17074 | Homo sapiens (human) | 23098 | SARM1 |
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| DOID:1289 | neurodegenerative disease | HGNC:17074 | Homo sapiens (human) | 23098 | SARM1 |
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| DOID:784 | chronic kidney disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:10787 | premature menopause | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:1289 | neurodegenerative disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:14717 | centronuclear myopathy | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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