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 |
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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 |
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DOID:11446 | sciatic neuropathy | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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DOID:824 | periodontitis | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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DOID:5844 | myocardial infarction | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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DOID:3070 | high grade glioma | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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DOID:1712 | aortic valve stenosis | RGD:2555 | Rattus norvegicus (Norway rat) | 25438 | Eno3 |
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DOID:2749 | glycogen storage disease Ia | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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DOID:14067 | Plasmodium falciparum malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:9744 | type 1 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:5844 | myocardial infarction | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:224 | transient cerebral ischemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:2383 | neonatal jaundice | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:557 | kidney disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:13413 | hepatic encephalopathy | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:1591 | renovascular hypertension | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:6713 | cerebrovascular disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:9281 | phenylketonuria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:684 | hepatocellular carcinoma | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:13628 | favism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024