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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 61901 - 61925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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:12849 autistic disorder HGNC:14295 Homo sapiens (human) 22941 SHANK2
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:14295 Homo sapiens (human) 22941 SHANK2
  • MGI:6194238
DOID:12849 autistic disorder HGNC:14291 Homo sapiens (human) 22871 NLGN1
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:14291 Homo sapiens (human) 22871 NLGN1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:14291 Homo sapiens (human) 22871 NLGN1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:14290 Homo sapiens (human) 57555 NLGN2
  • MGI:6194238
DOID:5419 schizophrenia HGNC:14290 Homo sapiens (human) 57555 NLGN2
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:14290 Homo sapiens (human) 57555 NLGN2
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:14290 Homo sapiens (human) 57555 NLGN2
  • MGI:6194238
DOID:12849 autistic disorder HGNC:14289 Homo sapiens (human) 54413 NLGN3
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:14289 Homo sapiens (human) 54413 NLGN3
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:14289 Homo sapiens (human) 54413 NLGN3
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:14287 Homo sapiens (human) 57502 NLGN4X
  • MGI:6194238
DOID:12849 autistic disorder HGNC:14287 Homo sapiens (human) 57502 NLGN4X
  • RGD:7240710

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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