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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:0070132 | autosomal recessive cutis laxa type IIIA | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0070131 | autosomal dominant cutis laxa 3 | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:1283 | enterocele | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0110825 | hereditary spastic paraplegia 9B | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0070143 | autosomal recessive cutis laxa type III | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:83 | cataract | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0050782 | Zollinger-Ellison syndrome | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:1240 | leukemia | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:13580 | cholestasis | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:13603 | obstructive jaundice | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:9538 | multiple myeloma | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:114 | heart disease | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:14089 | root caries | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:9675 | pulmonary emphysema | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:576 | proteinuria | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:12351 | alcoholic hepatitis | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:11266 | Hantavirus hemorrhagic fever with renal syndrome | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:0080600 | COVID-19 | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:1793 | pancreatic cancer | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:10591 | pre-eclampsia | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:0050625 | biliary tract benign neoplasm | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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