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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:13207 | proliferative diabetic retinopathy | RGD:69298 | Rattus norvegicus (Norway rat) | 84050 | Enpp2 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:0111305 | familial febrile seizures 4 | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:104 | bacterial infectious disease | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:0111839 | congenital disorder of glycosylation Icc | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:10283 | prostate cancer | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:0060545 | Hermansky-Pudlak syndrome 7 | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:2223 | platelet storage pool deficiency | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:5419 | schizophrenia | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:3753 | Hermansky-Pudlak syndrome | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:896 | metal metabolism disorder | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:1184 | nephrotic syndrome | HGNC:18816 | Homo sapiens (human) | 84063 | KIRREL2 |
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| DOID:557 | kidney disease | HGNC:18816 | Homo sapiens (human) | 84063 | KIRREL2 |
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| DOID:12336 | male infertility | HGNC:23045 | Homo sapiens (human) | 84071 | ARMC2 |
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| DOID:0111919 | spermatogenic failure 38 | HGNC:23045 | Homo sapiens (human) | 84071 | ARMC2 |
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| DOID:0080178 | mucositis | HGNC:12558 | Homo sapiens (human) | 8408 | ULK1 |
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| DOID:7004 | ACTH-secreting pituitary adenoma | MGI:1934029 | Mus musculus (house mouse) | 84092 | Usp8 |
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| DOID:0060774 | congenital diarrhea | MGI:1890497 | Mus musculus (house mouse) | 84094 | Plvap |
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| DOID:2785 | Dandy-Walker syndrome | HGNC:20393 | Homo sapiens (human) | 84107 | ZIC4 |
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| DOID:4621 | holoprosencephaly | HGNC:20393 | Homo sapiens (human) | 84107 | ZIC4 |
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| DOID:0080010 | bone structure disease | HGNC:15565 | Homo sapiens (human) | 84109 | QRFPR |
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