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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050709 | early infantile epileptic encephalopathy | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0112151 | corpus callosum agenesis-abnormal genitalia syndrome | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0080468 | developmental and epileptic encephalopathy 1 | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:1826 | epilepsy | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0112238 | X-linked lissencephaly 2 | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0112021 | non-syndromic X-linked intellectual disability ARX-related | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0050453 | lissencephaly | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:14744 | Partington syndrome | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0112038 | non-syndromic X-linked intellectual disability 1 | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:9455 | lipid storage disease | SGD:S000004232 | Saccharomyces cerevisiae S288C | 850943 | ARV1 |
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| DOID:0080417 | developmental and epileptic encephalopathy 38 | SGD:S000004232 | Saccharomyces cerevisiae S288C | 850943 | ARV1 |
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| DOID:574 | peripheral nervous system disease | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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| DOID:1793 | pancreatic cancer | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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| DOID:12689 | acoustic neuroma | HGNC:727 | Homo sapiens (human) | 9048 | ARTN |
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| DOID:2581 | chondrodysplasia punctata | HGNC:719 | Homo sapiens (human) | 415 | ARSL |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:719 | Homo sapiens (human) | 415 | ARSL |
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| DOID:12798 | mucopolysaccharidosis | HGNC:25239 | Homo sapiens (human) | 153642 | ARSK |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:12798 | mucopolysaccharidosis | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:714 | Homo sapiens (human) | 411 | ARSB |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
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