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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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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:13317 | hyperinsulinemic hypoglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:4195 | hyperglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:4194 | glucose metabolism disease | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:1682 | congenital heart disease | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:0050834 | CHARGE syndrome | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:0060041 | autism spectrum disorder | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:26178 | Homo sapiens (human) | 80206 | FHOD3 |
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| DOID:0110004 | 3-methylglutaconic aciduria type 3 | HGNC:8142 | Homo sapiens (human) | 80207 | OPA3 |
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| DOID:0111433 | optic atrophy 3 | HGNC:8142 | Homo sapiens (human) | 80207 | OPA3 |
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| DOID:0110176 | Charcot-Marie-Tooth disease axonal type 2X | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:0110764 | hereditary spastic paraplegia 11 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:0060197 | amyotrophic lateral sclerosis type 5 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:936 | brain disease | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:9119 | acute myeloid leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:10652 | Alzheimer's disease | HGNC:24128 | Homo sapiens (human) | 80213 | TM2D3 |
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| DOID:0070170 | spermatogenic failure 19 | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:1572 | normal pressure hydrocephalus | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:0111867 | nonphotosensitive trichothiodystrophy | HGNC:30740 | Homo sapiens (human) | 80222 | TARS2 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:30740 | Homo sapiens (human) | 80222 | TARS2 |
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| DOID:0111465 | combined oxidative phosphorylation deficiency 21 | HGNC:30740 | Homo sapiens (human) | 80222 | TARS2 |
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| DOID:162 | cancer | HGNC:30596 | Homo sapiens (human) | 80235 | PIGZ |
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| DOID:4927 | Klatskin's tumor | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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