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:8778 | Crohn's disease | FB:FBgn0026754 | Drosophila melanogaster (fruit fly) | 53583 | Ugt37C1 |
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DOID:9352 | type 2 diabetes mellitus | FB:FBgn0026754 | Drosophila melanogaster (fruit fly) | 53583 | Ugt37C1 |
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DOID:9744 | type 1 diabetes mellitus | FB:FBgn0026754 | Drosophila melanogaster (fruit fly) | 53583 | Ugt37C1 |
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DOID:1612 | breast cancer | FB:FBgn0026754 | Drosophila melanogaster (fruit fly) | 53583 | Ugt37C1 |
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DOID:9352 | type 2 diabetes mellitus | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:7998 | hyperthyroidism | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:3803 | Crigler-Najjar syndrome | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:2741 | bilirubin metabolic disorder | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:9744 | type 1 diabetes mellitus | FB:FBgn0026755 | Drosophila melanogaster (fruit fly) | 53584 | Ugt37B1 |
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DOID:9675 | pulmonary emphysema | MGI:1858901 | Mus musculus (house mouse) | 53618 | Fut8 |
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DOID:1289 | neurodegenerative disease | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:9114 | Homo sapiens (human) | 5372 | PMM1 |
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DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9114 | Homo sapiens (human) | 5372 | PMM1 |
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DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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DOID:9970 | obesity | HGNC:9155 | Homo sapiens (human) | 5406 | PNLIP |
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DOID:10283 | prostate cancer | HGNC:9156 | Homo sapiens (human) | 5407 | PNLIPRP1 |
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DOID:0080552 | congenital disorder of glycosylation Ia | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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DOID:5212 | congenital disorder of glycosylation | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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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