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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:5082 | liver cirrhosis | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:0111144 | preterm premature rupture of the membranes | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:10952 | nephritis | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:1793 | pancreatic cancer | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:557 | kidney disease | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:783 | end stage renal disease | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:12700 | hyperprolactinemia | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:9452 | steatotic liver disease | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:12308 | Dubin-Johnson syndrome | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:13580 | cholestasis | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:9119 | acute myeloid leukemia | HGNC:54 | Homo sapiens (human) | 8714 | ABCC3 |
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| DOID:0110521 | autosomal recessive nonsyndromic deafness 70 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:0111467 | combined oxidative phosphorylation deficiency 13 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:0050974 | spinocerebellar ataxia type 25 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:0112283 | spondyloepiphyseal dysplasia Kondo-Fu type | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:0110727 | neuronal ceroid lipofuscinosis 13 | HGNC:2531 | Homo sapiens (human) | 8722 | CTSF |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:2512 | Homo sapiens (human) | 8727 | CTNNAL1 |
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| DOID:0110202 | Charcot-Marie-Tooth disease dominant intermediate A | HGNC:4181 | Homo sapiens (human) | 8729 | GBF1 |
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| DOID:784 | chronic kidney disease | HGNC:1548 | Homo sapiens (human) | 873 | CBR1 |
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