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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:162 | cancer | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
|
||
| DOID:13533 | osteopetrosis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:0080162 | lupus nephritis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:9620 | vesicoureteral reflux | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:0080600 | COVID-19 | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:418 | systemic scleroderma | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:0111555 | Alkuraya-Kucinskas syndrome | SGD:S000004077 | Saccharomyces cerevisiae S288C | 850776 | CSF1 |
|
||
| DOID:783 | end stage renal disease | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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||
| DOID:3070 | high grade glioma | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:2921 | glomerulonephritis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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||
| DOID:9120 | amyloidosis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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||
| DOID:289 | endometriosis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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| DOID:13949 | interstitial cystitis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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||
| DOID:1936 | atherosclerosis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
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||
| DOID:1612 | breast cancer | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:2432 | Homo sapiens (human) | 1435 | CSF1 |
|
||
| DOID:0060041 | autism spectrum disorder | HGNC:29905 | Homo sapiens (human) | 7812 | CSDE1 |
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||
| DOID:1312 | focal segmental glomerulosclerosis | SGD:S000004231 | Saccharomyces cerevisiae S288C | 850942 | CSC1 |
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| DOID:0070456 | hereditary spastic paraplegia 87 | SGD:S000004231 | Saccharomyces cerevisiae S288C | 850942 | CSC1 |
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| DOID:331 | central nervous system disease | SGD:S000004231 | Saccharomyces cerevisiae S288C | 850942 | CSC1 |
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| DOID:0070400 | hypomyelinating leukodystrophy 19 | SGD:S000004231 | Saccharomyces cerevisiae S288C | 850942 | CSC1 |
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| DOID:8466 | retinal degeneration | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:7998 | hyperthyroidism | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:1459 | hypothyroidism | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
|
