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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 October 9, 2024
Displaying entries 71276 - 71300 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1574 alcohol use disorder HGNC:24124 Homo sapiens (human) 86 ACTL6A
  • MGI:6194238
DOID:10486 intestinal atresia HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
DOID:0081113 Baraitser-Winter syndrome 2 HGNC:144 Homo sapiens (human) 71 ACTG1
  • RGD:7240710
DOID:0081112 Baraitser-Winter syndrome 1 HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
DOID:0110550 autosomal dominant nonsyndromic deafness 20 HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
DOID:13099 Moyamoya disease HGNC:144 Homo sapiens (human) 71 ACTG1
  • MGI:6194238
DOID:13099 Moyamoya disease HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:0110317 hypertrophic cardiomyopathy 11 HGNC:143 Homo sapiens (human) 70 ACTC1
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:0110456 dilated cardiomyopathy 1R HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:143 Homo sapiens (human) 70 ACTC1
  • PMID:9563954
DOID:0110110 atrial heart septal defect 5 HGNC:143 Homo sapiens (human) 70 ACTC1
  • RGD:7240710
DOID:10763 hypertension HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:0110550 autosomal dominant nonsyndromic deafness 20 HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:0081112 Baraitser-Winter syndrome 1 HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:10486 intestinal atresia HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:3191 nemaline myopathy HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:143 Homo sapiens (human) 70 ACTC1
  • MGI:6194238
DOID:0081112 Baraitser-Winter syndrome 1 HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238
DOID:14004 thoracic aortic aneurysm HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238
DOID:10486 intestinal atresia HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238
DOID:13099 Moyamoya disease HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238

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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


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Last updated: December 9, 2024