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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:8947 | diabetic retinopathy | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:8466 | retinal degeneration | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:1407 | anterior uveitis | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:4448 | macular degeneration | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:29368 | Homo sapiens (human) | 85452 | CFAP74 |
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| DOID:0111918 | spermatogenic failure 40 | HGNC:25325 | Homo sapiens (human) | 255101 | CFAP65 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:15872 | Homo sapiens (human) | 26074 | CFAP61 |
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| DOID:0112271 | spermatogenic failure 49 | HGNC:26676 | Homo sapiens (human) | 159686 | CFAP58 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:26676 | Homo sapiens (human) | 159686 | CFAP58 |
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| DOID:0050545 | visceral heterotaxy | HGNC:26530 | Homo sapiens (human) | 220136 | CFAP53 |
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| DOID:12336 | male infertility | HGNC:26708 | Homo sapiens (human) | 286464 | CFAP47 |
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| DOID:0112274 | X-linked spermatogenic failure 3 | HGNC:26708 | Homo sapiens (human) | 286464 | CFAP47 |
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| DOID:0070166 | spermatogenic failure 20 | HGNC:25631 | Homo sapiens (human) | 55779 | CFAP44 |
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| DOID:0070170 | spermatogenic failure 19 | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:1572 | normal pressure hydrocephalus | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:0111155 | autosomal recessive spinocerebellar ataxia 21 | SGD:S000005638 | Saccharomyces cerevisiae S288C | 854279 | CEX1 |
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| DOID:0050951 | hereditary ataxia | SGD:S000005638 | Saccharomyces cerevisiae S288C | 854279 | CEX1 |
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| DOID:0111369 | hyperalphalipoproteinemia 1 | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
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| DOID:3407 | carotid artery disease | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
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| DOID:9256 | colorectal cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:10534 | stomach cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:3119 | gastrointestinal system cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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