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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 71751 - 71775 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10584 retinitis pigmentosa HGNC:34 Homo sapiens (human) 24 ABCA4
  • PMID:18024811
  • PMID:9466990
DOID:0060041 autism spectrum disorder HGNC:33 Homo sapiens (human) 21 ABCA3
  • MGI:6194238
DOID:12120 pulmonary alveolar proteinosis HGNC:33 Homo sapiens (human) 21 ABCA3
  • MGI:6194238
  • RGD:7240710
DOID:3717 gastric adenocarcinoma HGNC:14638 Homo sapiens (human) 154664 ABCA13
  • PMID:27366209
DOID:0060712 autosomal recessive congenital ichthyosis 4A HGNC:14637 Homo sapiens (human) 26154 ABCA12
  • RGD:7240710
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:14637 Homo sapiens (human) 26154 ABCA12
  • MGI:6194238
  • RGD:7240710
DOID:0060656 autosomal recessive congenital ichthyosis 1 HGNC:14637 Homo sapiens (human) 26154 ABCA12
  • PMID:12915478
DOID:10787 premature menopause HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:9970 obesity HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
  • PMID:17287470
DOID:9352 type 2 diabetes mellitus HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:18003760
DOID:783 end stage renal disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:10230 aortic atherosclerosis HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:33035679
DOID:1168 familial hyperlipidemia HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:1388 Tangier disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
  • PMID:10431236
  • PMID:11086027
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:11086027
DOID:10976 membranous glomerulonephritis HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
  • PMID:30580964
DOID:0080957 primary hypoalphalipoproteinemia 1 HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:10431236
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:15024730
DOID:1387 hypolipoproteinemia HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:11086027
DOID:12236 primary biliary cholangitis HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:28660384
DOID:13619 extrahepatic cholestasis HGNC:29 Homo sapiens (human) 19 ABCA1
  • MGI:6194238
DOID:326 ischemia HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:9976 heroin dependence HGNC:23 Homo sapiens (human) 18 ABAT
  • 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: December 9, 2024