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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 8501 - 8525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5138 leiomyomatosis HGNC:3700 Homo sapiens (human) 2271 FH
  • MGI:6194238
DOID:3805 porokeratosis HGNC:3631 Homo sapiens (human) 2224 FDPS
  • RGD:7240710
DOID:83 cataract HGNC:3629 Homo sapiens (human) 2222 FDFT1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:3622 Homo sapiens (human) 2218 FKTN
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:3622 Homo sapiens (human) 2218 FKTN
  • MGI:6194238
  • PMID:11445638
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:3622 Homo sapiens (human) 2218 FKTN
  • PMID:10545611
  • PMID:19266496
  • PMID:9690476
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L HGNC:3622 Homo sapiens (human) 2218 FKTN
  • PMID:17044012
DOID:0110444 dilated cardiomyopathy 1X HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:0110443 dilated cardiomyopathy 1B HGNC:3622 Homo sapiens (human) 2218 FKTN
  • PMID:17036286
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:9884 muscular dystrophy HGNC:3622 Homo sapiens (human) 2218 FKTN
  • PMID:10852541
  • PMID:19179078
  • PMID:19342235
  • PMID:20961758
DOID:5204 fructose-1,6-bisphosphatase deficiency HGNC:3606 Homo sapiens (human) 2203 FBP1
  • PMID:7763253
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:3594 Homo sapiens (human) 2194 FASN
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:3594 Homo sapiens (human) 2194 FASN
  • PMID:32525817
DOID:0080000 muscular disease HGNC:3594 Homo sapiens (human) 2194 FASN
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:3575 Homo sapiens (human) 9415 FADS2
  • PMID:24284026
DOID:9744 type 1 diabetes mellitus HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:5804 discrete subaortic stenosis HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:9970 obesity HGNC:3574 Homo sapiens (human) 3992 FADS1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:3574 Homo sapiens (human) 3992 FADS1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:3574 Homo sapiens (human) 3992 FADS1
  • 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