Table Filtering
Other Information
Release Statistics Download
Guidelines
MIRAGE
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 January 28, 2025
Displaying entries 8726 - 8750 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:0111131 focal segmental glomerulosclerosis 6 HGNC:7599 Homo sapiens (human) 4643 MYO1E inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:7595 Homo sapiens (human) 4640 MYO1A inference by association of genotype from phenotype used in manual assertion
  • PMID:12736868
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • PMID:19706030
DOID:14004 thoracic aortic aneurysm HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11394 adult respiratory distress syndrome HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • PMID:18828194
DOID:2841 asthma HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • PMID:17472811
DOID:14004 thoracic aortic aneurysm HGNC:7569 Homo sapiens (human) 4629 MYH11 inference by association of genotype from phenotype used in manual assertion
  • PMID:16444274
  • RGD:7240710
DOID:13832 patent ductus arteriosus HGNC:7569 Homo sapiens (human) 4629 MYH11 inference by association of genotype from phenotype used in manual assertion
  • PMID:16444274
  • PMID:27418595
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:7569 Homo sapiens (human) 4629 MYH11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:783 end stage renal disease HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:18794854
  • PMID:19177153
  • PMID:19567477
  • PMID:20144966
  • PMID:21968013
DOID:0110548 autosomal dominant nonsyndromic deafness 17 HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:10973259
DOID:10003 sensorineural hearing loss HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:26226608
DOID:0110032 autosomal dominant Alport syndrome HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:12500226
DOID:576 proteinuria HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:20200500
  • PMID:21910715
DOID:0050567 orofacial cleft HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:17337617
  • PMID:18716610
  • PMID:19320731
  • PMID:19891592
DOID:0060651 MYH-9 related disease HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:11752022
  • PMID:11935325
  • PMID:16806139
  • RGD:7240710
DOID:0070197 distal myopathy 1 HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • PMID:15358028
  • PMID:15856146
  • PMID:9154300
DOID:0111269 autosomal dominant hyaline body myopathy HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • PMID:14520662
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • PMID:11106718
DOID:0111268 autosomal recessive hyaline body myopathy HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110307 hypertrophic cardiomyopathy 1 HGNC:7577 Homo sapiens (human) 4625 MYH7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9955 hypoplastic left heart syndrome HGNC:7577 Homo sapiens (human) 4625 MYH7 genetic interaction evidence used in manual assertion
  • PMID:27789736

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025