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:6000 | congestive heart failure | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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DOID:10763 | hypertension | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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DOID:9256 | colorectal cancer | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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DOID:0080000 | muscular disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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DOID:5204 | fructose-1,6-bisphosphatase deficiency | SGD:S000004369 | Saccharomyces cerevisiae S288C | 851092 | FBP1 |
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DOID:5204 | fructose-1,6-bisphosphatase deficiency | HGNC:3606 | Homo sapiens (human) | 2203 | FBP1 |
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DOID:2018 | hyperinsulinism | SGD:S000003691 | Saccharomyces cerevisiae S288C | 853286 | FBP26 |
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DOID:83 | cataract | HGNC:3629 | Homo sapiens (human) | 2222 | FDFT1 |
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DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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DOID:5138 | leiomyomatosis | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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DOID:1289 | neurodegenerative disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0060202 | amyotrophic lateral sclerosis type 11 | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:0110184 | Charcot-Marie-Tooth disease type 4J | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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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