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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 5676 - 5700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus HGNC:9291 Homo sapiens (human) 5506 PPP1R3A
  • MGI:6194238
  • PMID:10389856
  • PMID:10868947
  • PMID:11793847
  • PMID:12831406
  • PMID:19553562
  • PMID:9653600
  • PMID:9726244
  • RGD:7240710
DOID:9993 hypoglycemia HGNC:9291 Homo sapiens (human) 5506 PPP1R3A
  • PMID:9814479
DOID:1574 alcohol use disorder HGNC:9293 Homo sapiens (human) 5507 PPP1R3C
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:9293 Homo sapiens (human) 5507 PPP1R3C
  • MGI:6194238
DOID:9970 obesity HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:7617578
DOID:14723 beta-ketothiolase deficiency HGNC:93 Homo sapiens (human) 38 ACAT1
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:15961705
DOID:783 end stage renal disease HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:0080738 Ehlers-Danlos syndrome spondylodysplastic type 1 HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • MGI:6194238
  • PMID:10473568
DOID:0014667 disease of metabolism HGNC:932 Homo sapiens (human) 570 BAAT
  • PMID:12704386
DOID:14503 neuronal ceroid lipofuscinosis HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
DOID:0110721 neuronal ceroid lipofuscinosis 1 HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
  • RGD:7240710
DOID:0110731 neuronal ceroid lipofuscinosis 3 HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
DOID:14503 neuronal ceroid lipofuscinosis HGNC:9326 Homo sapiens (human) 9374 PPT2
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:24645842
DOID:11832 visual epilepsy HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:15851405
DOID:3669 intermittent claudication HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:21918885
  • PMID:24092988
DOID:0081292 traumatic brain injury HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:9970 obesity HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:10763 hypertension HGNC:936 Homo sapiens (human) 572 BAD
  • 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