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 | October 9, 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:1574 | alcohol use disorder | RGD:69426 | Rattus norvegicus (Norway rat) | 29335 | Oprk1 |
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DOID:1574 | alcohol use disorder | RGD:3233 | Rattus norvegicus (Norway rat) | 24613 | Oprd1 |
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DOID:13133 | HELLP syndrome | RGD:619831 | Rattus norvegicus (Norway rat) | 246097 | Fas |
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DOID:13133 | HELLP syndrome | RGD:3880 | Rattus norvegicus (Norway rat) | 25385 | Faslg |
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DOID:10652 | Alzheimer's disease | FB:FBgn0039234 | Drosophila melanogaster (fruit fly) | 42964 | Nct |
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DOID:11252 | microcytic anemia | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | MGI:103264 | Mus musculus (house mouse) | 16800 | Arhgef2 |
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DOID:1596 | depressive disorder | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
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DOID:1596 | depressive disorder | RGD:621544 | Rattus norvegicus (Norway rat) | 171131 | Chrnb3 |
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DOID:0110673 | congenital myasthenic syndrome 19 | MGI:1277201 | Mus musculus (house mouse) | 12817 | Col13a1 |
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DOID:0080092 | myofibrillar myopathy 1 | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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DOID:12801 | mucopolysaccharidosis III | MGI:1922862 | Mus musculus (house mouse) | 75612 | Gns |
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DOID:10652 | Alzheimer's disease | HGNC:8824 | Homo sapiens (human) | 5176 | SERPINF1 |
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DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | HGNC:10806 | Homo sapiens (human) | 6443 | SGCB |
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DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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DOID:9452 | steatotic liver disease | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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DOID:9452 | steatotic liver disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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DOID:10652 | Alzheimer's disease | RGD:70514 | Rattus norvegicus (Norway rat) | 140908 | Cdk5 |
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DOID:0080195 | Marinesco-Sjogren syndrome | SGD:S000005391 | Saccharomyces cerevisiae S288C | 854126 | SIL1 |
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DOID:898 | autosomal dominant polycystic kidney disease | MGI:1099818 | Mus musculus (house mouse) | 18764 | Pkd2 |
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DOID:3883 | Lynch syndrome | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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DOID:684 | hepatocellular carcinoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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DOID:6432 | pulmonary hypertension | RGD:631365 | Rattus norvegicus (Norway rat) | 297508 | Nampt |
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DOID:6432 | pulmonary hypertension | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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DOID:0070113 | Niemann-Pick disease type C1 | MGI:1097712 | Mus musculus (house mouse) | 18145 | Npc1 |
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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 v4.1.0
Last updated: December 9, 2024