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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:10283 | prostate cancer | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:3070 | high grade glioma | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:5419 | schizophrenia | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:12849 | autistic disorder | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:12858 | Huntington's disease | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:1742 | Homo sapiens (human) | 987 | LRBA |
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| DOID:0081151 | common variable immunodeficiency 8 | HGNC:1742 | Homo sapiens (human) | 987 | LRBA |
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| DOID:0060438 | Cole-Carpenter syndrome | HGNC:10706 | Homo sapiens (human) | 9871 | SEC24D |
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| DOID:0110717 | Warburg micro syndrome 2 | MGI:1916043 | Mus musculus (house mouse) | 98732 | Rab3gap2 |
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| DOID:0111586 | Martsolf syndrome | MGI:1916043 | Mus musculus (house mouse) | 98732 | Rab3gap2 |
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| DOID:0060237 | Warburg micro syndrome | MGI:1916043 | Mus musculus (house mouse) | 98732 | Rab3gap2 |
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| DOID:0050741 | alcohol dependence | MGI:99632 | Mus musculus (house mouse) | 98741 | Kcnb2 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:1743 | Homo sapiens (human) | 988 | CDC5L |
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| DOID:1574 | alcohol use disorder | HGNC:1743 | Homo sapiens (human) | 988 | CDC5L |
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| DOID:3347 | osteosarcoma | HGNC:1743 | Homo sapiens (human) | 988 | CDC5L |
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| DOID:3138 | acanthosis nigricans | HGNC:19165 | Homo sapiens (human) | 9882 | TBC1D4 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:14986 | Homo sapiens (human) | 9892 | SNAP91 |
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| DOID:10652 | Alzheimer's disease | HGNC:14986 | Homo sapiens (human) | 9892 | SNAP91 |
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| DOID:0110801 | hereditary spastic paraplegia 49 | HGNC:19957 | Homo sapiens (human) | 9895 | TECPR2 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | 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:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:1289 | neurodegenerative disease | 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:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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