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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 1551 - 1575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:4247 coronary restenosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18387661
DOID:11054 urinary bladder cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18094410
DOID:162 cancer HGNC:1769 Homo sapiens (human) 10423 CDIPT
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:1769 Homo sapiens (human) 10423 CDIPT
  • MGI:6194238
DOID:162 cancer SGD:S000000233 Saccharomyces cerevisiae S288C 852317 CDS1
  • PMID:26354769
DOID:162 cancer HGNC:1800 Homo sapiens (human) 1040 CDS1
  • MGI:6194238
DOID:162 cancer HGNC:1801 Homo sapiens (human) 8760 CDS2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:16369531
DOID:9744 type 1 diabetes mellitus HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:10580419
  • PMID:9536927
DOID:3153 lipomatosis HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:17259390
DOID:0111105 maturity-onset diabetes of the young type 8 HGNC:1848 Homo sapiens (human) 1056 CEL
  • RGD:7240710
DOID:5679 retinal disease HGNC:24289 Homo sapiens (human) 10390 CEPT1
  • MGI:6194238
DOID:0111451 progressive myoclonus epilepsy 8 HGNC:14253 Homo sapiens (human) 10715 CERS1
  • RGD:7240710
DOID:11446 sciatic neuropathy HGNC:14076 Homo sapiens (human) 29956 CERS2
  • MGI:6194238
DOID:0060718 autosomal recessive congenital ichthyosis 9 HGNC:23752 Homo sapiens (human) 204219 CERS3
  • RGD:7240710
DOID:0060770 dextro-looped transposition of the great arteries HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:6406 double outlet right ventricle HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:0060856 right atrial isomerism HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:0050545 visceral heterotaxy HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
  • RGD:7240710
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q FB:FBgn0039827 Drosophila melanogaster (fruit fly) 43689 CG1544
  • MGI:6194238
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria FB:FBgn0039827 Drosophila melanogaster (fruit fly) 43689 CG1544
  • MGI:6194238
DOID:12930 dilated cardiomyopathy FB:FBgn0034567 Drosophila melanogaster (fruit fly) 37375 CG15651 CG15651
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 FB:FBgn0034567 Drosophila melanogaster (fruit fly) 37375 CG15651 CG15651
  • MGI:6194238
DOID:0111241 congenital muscular dystrophy-dystroglycanopathy type A5 FB:FBgn0034567 Drosophila melanogaster (fruit fly) 37375 CG15651 CG15651
  • 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: August 19, 2024