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:4247 | coronary restenosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:10283 | prostate cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:11054 | urinary bladder cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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DOID:162 | cancer | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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DOID:9452 | steatotic liver disease | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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DOID:162 | cancer | SGD:S000000233 | Saccharomyces cerevisiae S288C | 852317 | CDS1 |
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DOID:162 | cancer | HGNC:1800 | Homo sapiens (human) | 1040 | CDS1 |
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DOID:162 | cancer | HGNC:1801 | Homo sapiens (human) | 8760 | CDS2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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DOID:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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DOID:5679 | retinal disease | HGNC:24289 | Homo sapiens (human) | 10390 | CEPT1 |
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DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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DOID:6406 | double outlet right ventricle | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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DOID:0060856 | right atrial isomerism | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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DOID:0050545 | visceral heterotaxy | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | FB:FBgn0039827 | Drosophila melanogaster (fruit fly) | 43689 | CG1544 |
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DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | FB:FBgn0039827 | Drosophila melanogaster (fruit fly) | 43689 | CG1544 |
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DOID:12930 | dilated cardiomyopathy | FB:FBgn0034567 | Drosophila melanogaster (fruit fly) | 37375 | CG15651 | CG15651 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | FB:FBgn0034567 | Drosophila melanogaster (fruit fly) | 37375 | CG15651 | CG15651 |
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DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | FB:FBgn0034567 | Drosophila melanogaster (fruit fly) | 37375 | CG15651 | CG15651 |
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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