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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:557 | kidney disease | HGNC:9844 | Homo sapiens (human) | 10266 | RAMP2 |
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| DOID:9256 | colorectal cancer | HGNC:9844 | Homo sapiens (human) | 10266 | RAMP2 |
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| DOID:10763 | hypertension | HGNC:9844 | Homo sapiens (human) | 10266 | RAMP2 |
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| DOID:6000 | congestive heart failure | HGNC:9844 | Homo sapiens (human) | 10266 | RAMP2 |
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| DOID:1793 | pancreatic cancer | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:5768 | Nager acrofacial dysostosis | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:4362 | cervical cancer | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:0080564 | congenital disorder of glycosylation Il | MGI:1924753 | Mus musculus (house mouse) | 102580 | Alg9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1924753 | Mus musculus (house mouse) | 102580 | Alg9 |
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| DOID:13580 | cholestasis | HGNC:55 | Homo sapiens (human) | 10257 | ABCC4 |
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| DOID:13619 | extrahepatic cholestasis | HGNC:55 | Homo sapiens (human) | 10257 | ABCC4 |
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| DOID:1485 | cystic fibrosis | HGNC:55 | Homo sapiens (human) | 10257 | ABCC4 |
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| DOID:0080322 | polycystic kidney disease | HGNC:11358 | Homo sapiens (human) | 10254 | STAM2 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:0060340 | ciliopathy | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:0080072 | intestinal pseudo-obstruction | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:9164 | achalasia | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:11714 | gestational diabetes | HGNC:16638 | Homo sapiens (human) | 10250 | SRRM1 |
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| DOID:0050857 | Perrault syndrome | MGI:2142973 | Mus musculus (house mouse) | 102436 | Lars2 |
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| DOID:700 | mitochondrial metabolism disease | MGI:2142973 | Mus musculus (house mouse) | 102436 | Lars2 |
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| DOID:0111166 | molybdenum cofactor deficiency type C | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:655 | inherited metabolic disorder | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:1779 | Homo sapiens (human) | 1024 | CDK8 |
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| DOID:0112221 | developmental and epileptic encephalopathy 87 | HGNC:1779 | Homo sapiens (human) | 1024 | CDK8 |
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