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:557 | kidney disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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DOID:594 | panic disorder | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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DOID:9352 | type 2 diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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DOID:3304 | germinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:3748 | esophagus squamous cell carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:0050773 | paraganglioma | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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DOID:0050861 | colorectal adenocarcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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DOID:0081001 | Cowden syndrome 5 | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:9252 | amino acid metabolic disorder | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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DOID:5844 | myocardial infarction | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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DOID:874 | bacterial pneumonia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:0110312 | hypertrophic cardiomyopathy 6 | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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DOID:3407 | carotid artery disease | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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DOID:399 | tuberculosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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DOID:1993 | rectum cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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DOID:10892 | hypospadias | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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DOID:9976 | heroin dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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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