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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:9744 | type 1 diabetes mellitus | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:14219 | renal tubular acidosis | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:2355 | anemia | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:10763 | hypertension | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:4947 | cholangiocarcinoma | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:14330 | Parkinson's disease | HGNC:3298 | Homo sapiens (human) | 8672 | EIF4G3 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | FB:FBgn0259933 | Drosophila melanogaster (fruit fly) | 8674033 | Dpm2 | CG42456 |
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| DOID:0080176 | meningococcal meningitis | HGNC:6895 | Homo sapiens (human) | 8685 | MARCO |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6895 | Homo sapiens (human) | 8685 | MARCO |
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| DOID:10325 | silicosis | HGNC:6895 | Homo sapiens (human) | 8685 | MARCO |
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| DOID:6432 | pulmonary hypertension | HGNC:5321 | Homo sapiens (human) | 8692 | HYAL2 |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:9970 | obesity | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:784 | chronic kidney disease | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:5223 | infertility | HGNC:1724 | Homo sapiens (human) | 8697 | CDC23 |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:163 | Homo sapiens (human) | 87 | ACTN1 |
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| DOID:0111053 | platelet-type bleeding disorder 15 | HGNC:163 | Homo sapiens (human) | 87 | ACTN1 |
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| DOID:0110605 | primary ciliary dyskinesia 7 | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0050545 | visceral heterotaxy | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0050144 | Kartagener syndrome | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0050651 | atrioventricular septal defect | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0110346 | osteogenesis imperfecta type 10 | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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