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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:583 | hemolytic anemia | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:585 | nephrolithiasis | HGNC:16262 | Homo sapiens (human) | 10413 | YAP1 |
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| DOID:9362 | status asthmaticus | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:0070133 | autosomal recessive cutis laxa type IB | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
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| DOID:12236 | primary biliary cholangitis | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:3526 | cerebral infarction | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:6000 | congestive heart failure | HGNC:2654 | Homo sapiens (human) | 3491 | CCN1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9293 | Homo sapiens (human) | 5507 | PPP1R3C |
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| DOID:9261 | nasopharynx carcinoma | HGNC:9801 | Homo sapiens (human) | 5879 | RAC1 |
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| DOID:2349 | arteriosclerosis | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:362 | Homo sapiens (human) | 204 | AK2 |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0050700 | cardiomyopathy | HGNC:4468 | Homo sapiens (human) | 2837 | UTS2R |
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| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:3942 | Homo sapiens (human) | 2475 | MTOR |
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| DOID:6000 | congestive heart failure | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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| DOID:0070444 | neurodevelopmental disorder with language delay and seizures | HGNC:11805 | Homo sapiens (human) | 7074 | TIAM1 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:10610 | Homo sapiens (human) | 6356 | CCL11 |
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| DOID:9505 | cannabis abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:10907 | microcephaly | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
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| DOID:4465 | papillary renal cell carcinoma | HGNC:9343 | Homo sapiens (human) | 5546 | PRCC |
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| DOID:5213 | chronic inflammatory demyelinating polyradiculoneuropathy | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:17071 | Homo sapiens (human) | 23081 | KDM4C |
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| DOID:3070 | high grade glioma | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:0050157 | cryptogenic organizing pneumonia | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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