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:3525 | middle cerebral artery infarction | FB:FBgn0001092 | Drosophila melanogaster (fruit fly) | 32545 | Gapdh2 |
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DOID:13088 | periventricular leukomalacia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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DOID:5016 | hepatocellular clear cell carcinoma | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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DOID:9256 | colorectal cancer | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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DOID:9256 | colorectal cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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DOID:10652 | Alzheimer's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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DOID:2349 | arteriosclerosis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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DOID:3407 | carotid artery disease | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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DOID:0112298 | spondylometaphyseal dysplasia Sedaghatian type | SGD:S000001509 | Saccharomyces cerevisiae S288C | 853842 | GPX1 |
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DOID:12798 | mucopolysaccharidosis | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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DOID:10591 | pre-eclampsia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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DOID:3146 | lipid metabolism disorder | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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DOID:5844 | myocardial infarction | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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DOID:0110645 | long QT syndrome 2 | RGD:708500 | Rattus norvegicus (Norway rat) | 245960 | Alg10 |
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DOID:0080855 | Parkinsonism | SGD:S000005920 | Saccharomyces cerevisiae S288C | 854575 | ERR1 |
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DOID:4079 | heart valve disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:5212 | congenital disorder of glycosylation | ZFIN:ZDB-GENE-061013-84 | Danio rerio (zebrafish) | 768123 | b4galt1l |
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DOID:8893 | psoriasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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DOID:1574 | alcohol use disorder | RGD:3676 | Rattus norvegicus (Norway rat) | 25197 | St6gal1 |
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DOID:11400 | pyelonephritis | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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DOID:0080561 | congenital disorder of glycosylation Ii | ZFIN:ZDB-GENE-060502-2 | Danio rerio (zebrafish) | 403068 | alg2 |
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DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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DOID:684 | hepatocellular carcinoma | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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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