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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 71301 - 71325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0110550 autosomal dominant nonsyndromic deafness 20 HGNC:17780 Homo sapiens (human) 345651 ACTBL2
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:10881 hand, foot and mouth disease HGNC:132 Homo sapiens (human) 60 ACTB
  • PMID:30817906
DOID:1588 thrombocytopenia HGNC:132 Homo sapiens (human) 60 ACTB
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:0110317 hypertrophic cardiomyopathy 11 HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:0110550 autosomal dominant nonsyndromic deafness 20 HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:3328 temporal lobe epilepsy HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:423 myopathy HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:0081112 Baraitser-Winter syndrome 1 HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
  • RGD:7240710
DOID:422 congenital structural myopathy HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:13099 Moyamoya disease HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:3191 nemaline myopathy HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:10486 intestinal atresia HGNC:132 Homo sapiens (human) 60 ACTB
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
DOID:10486 intestinal atresia HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
DOID:4977 lymphedema HGNC:130 Homo sapiens (human) 59 ACTA2
  • PMID:21510802
DOID:0081112 Baraitser-Winter syndrome 1 HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
DOID:13099 Moyamoya disease HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
  • RGD:7240710
DOID:0110550 autosomal dominant nonsyndromic deafness 20 HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
DOID:0050827 rheumatic heart disease HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
DOID:14004 thoracic aortic aneurysm HGNC:130 Homo sapiens (human) 59 ACTA2
  • MGI:6194238
  • PMID:19639654
  • PMID:21212136
  • RGD:7240710
DOID:0080685 aortic dissection HGNC:129 Homo sapiens (human) 58 ACTA1
  • PMID:28167124

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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: December 9, 2024