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Alliance of Genome Resources

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
Alliance of Genome Resources July 29, 2024
Displaying entries 701 - 725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:557 kidney disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:15983323
  • PMID:16928730
DOID:594 panic disorder HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24856568
DOID:0060230 basal ganglia calcification HGNC:19918 Homo sapiens (human) 57462 MYORG
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:11996959
DOID:3304 germinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:19289622
DOID:3748 esophagus squamous cell carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:15205355
  • PMID:25162968
DOID:0060227 Adams-Oliver syndrome HGNC:28526 Homo sapiens (human) 285203 EOGT
  • RGD:7240710
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4801 Homo sapiens (human) 3030 HADHA
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:27214654
DOID:0050773 paraganglioma HGNC:2911 Homo sapiens (human) 1743 DLST
  • RGD:7240710
DOID:0050861 colorectal adenocarcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:28009432
DOID:0081001 Cowden syndrome 5 HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:9252 amino acid metabolic disorder HGNC:8654 Homo sapiens (human) 5096 PCCB
  • PMID:8411997
DOID:0050770 polycystic liver disease HGNC:23161 Homo sapiens (human) 79053 ALG8
  • RGD:7240710
DOID:0111043 glycogen storage disease IXc HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:18549840
DOID:0112347 hereditary spastic paraplegia 84 HGNC:8983 Homo sapiens (human) 5297 PI4KA
  • RGD:7240710
DOID:874 bacterial pneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18641104
DOID:0110312 hypertrophic cardiomyopathy 6 HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • RGD:7240710
DOID:3407 carotid artery disease HGNC:9592 Homo sapiens (human) 5730 PTGDS
  • PMID:15325247
DOID:399 tuberculosis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • RGD:7240710
DOID:1993 rectum cancer HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:22371331
DOID:10892 hypospadias HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:14764821
DOID:9976 heroin dependence HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:21723677

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024