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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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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:3525 | middle cerebral artery infarction | MGI:1929865 | Mus musculus (house mouse) | 59027 | Nampt |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:1929865 | Mus musculus (house mouse) | 59027 | Nampt |
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| DOID:1074 | kidney failure | MGI:1929865 | Mus musculus (house mouse) | 59027 | Nampt |
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| DOID:3407 | carotid artery disease | MGI:1929865 | Mus musculus (house mouse) | 59027 | Nampt |
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| DOID:0050731 | vitamin B12 deficiency | RGD:2639 | Rattus norvegicus (Norway rat) | 58924 | Fut2 |
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| DOID:3910 | lung adenocarcinoma | MGI:1929955 | Mus musculus (house mouse) | 58810 | Akr1a1 |
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| DOID:1612 | breast cancer | MGI:1929955 | Mus musculus (house mouse) | 58810 | Akr1a1 |
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| DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:13580 | cholestasis | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:3650 | lactic acidosis | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2754 | glycogen storage disease VI | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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| DOID:557 | kidney disease | HGNC:19069 | Homo sapiens (human) | 57733 | GBA3 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:1184 | nephrotic syndrome | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:9970 | obesity | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:4947 | cholangiocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1824 | status epilepticus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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