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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9538 | multiple myeloma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:12858 | Huntington's disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:11714 | gestational diabetes | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050083 | Keshan disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1289 | neurodegenerative disease | RGD:1310078 | Rattus norvegicus (Norway rat) | 287545 | Sarm1 |
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| DOID:332 | amyotrophic lateral sclerosis | RGD:1310078 | Rattus norvegicus (Norway rat) | 287545 | Sarm1 |
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| DOID:10534 | stomach cancer | RGD:628731 | Rattus norvegicus (Norway rat) | 286971 | Fut11 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:10763 | hypertension | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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| DOID:6432 | pulmonary hypertension | RGD:708528 | Rattus norvegicus (Norway rat) | 282821 | Has1 |
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| DOID:6432 | pulmonary hypertension | ZFIN:ZDB-GENE-021118-1 | Danio rerio (zebrafish) | 282555 | has3 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:14330 | Parkinson's disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9119 | acute myeloid leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:440 | neuromuscular disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:114 | heart disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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