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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:2349 | arteriosclerosis | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:11520 | benign hypertensive renal disease | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:784 | chronic kidney disease | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:5844 | myocardial infarction | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:0111787 | frontometaphyseal dysplasia 2 | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:10283 | prostate cancer | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0050453 | lissencephaly | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:9884 | muscular dystrophy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0050667 | alcohol-related neurodevelopmental disorder | MGI:1916125 | Mus musculus (house mouse) | 68875 | Tmcc2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:10273 | heart conduction disease | RGD:1582911 | Rattus norvegicus (Norway rat) | 688996 | Kcnk16 |
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| DOID:114 | heart disease | RGD:1582911 | Rattus norvegicus (Norway rat) | 688996 | Kcnk16 |
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| DOID:1826 | epilepsy | RGD:1582911 | Rattus norvegicus (Norway rat) | 688996 | Kcnk16 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:1205 | allergic disease | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:2841 | asthma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
|
