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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:0060399 | chromosome 16p12.1 deletion syndrome | MGI:1914253 | Mus musculus (house mouse) | 67003 | Uqcrc2 |
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| DOID:162 | cancer | MGI:1914302 | Mus musculus (house mouse) | 67052 | Ndc80 |
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| DOID:9256 | colorectal cancer | MGI:1914302 | Mus musculus (house mouse) | 67052 | Ndc80 |
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| DOID:3908 | lung non-small cell carcinoma | MGI:1914302 | Mus musculus (house mouse) | 67052 | Ndc80 |
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| DOID:10534 | stomach cancer | MGI:1914302 | Mus musculus (house mouse) | 67052 | Ndc80 |
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| DOID:5419 | schizophrenia | MGI:1914304 | Mus musculus (house mouse) | 67054 | Paics |
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| DOID:104 | bacterial infectious disease | MGI:1914325 | Mus musculus (house mouse) | 67075 | Magt1 |
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| DOID:0111839 | congenital disorder of glycosylation Icc | MGI:1914325 | Mus musculus (house mouse) | 67075 | Magt1 |
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| DOID:10283 | prostate cancer | MGI:1914325 | Mus musculus (house mouse) | 67075 | Magt1 |
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| DOID:612 | primary immunodeficiency disease | MGI:1914325 | Mus musculus (house mouse) | 67075 | Magt1 |
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| DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | MGI:1914325 | Mus musculus (house mouse) | 67075 | Magt1 |
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| DOID:0110916 | hereditary spherocytosis type 1 | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:10923 | sickle cell anemia | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:0110918 | hereditary spherocytosis type 3 | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:12971 | hereditary spherocytosis | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:0080438 | developmental and epileptic encephalopathy 5 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
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| DOID:0081400 | autosomal dominant distal hereditary motor neuronopathy 11 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
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| DOID:0112204 | developmental and epileptic encephalopathy 68 | MGI:1914345 | Mus musculus (house mouse) | 67095 | Trak1 |
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| DOID:13366 | Stiff-Person syndrome | MGI:1914345 | Mus musculus (house mouse) | 67095 | Trak1 |
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| DOID:1289 | neurodegenerative disease | MGI:1914345 | Mus musculus (house mouse) | 67095 | Trak1 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1095 | Homo sapiens (human) | 671 | BPI |
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| DOID:8778 | Crohn's disease | HGNC:1095 | Homo sapiens (human) | 671 | BPI |
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| DOID:0110917 | hereditary spherocytosis type 2 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:12971 | hereditary spherocytosis | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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