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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 71626 - 71650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0060639 permanent neonatal diabetes mellitus HGNC:59 Homo sapiens (human) 6833 ABCC8
  • RGD:7240710
DOID:0060319 cardiac arrest HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:13317 hyperinsulinemic hypoglycemia HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0060334 transient neonatal diabetes mellitus HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:10763 hypertension HGNC:59 Homo sapiens (human) 6833 ABCC8
  • PMID:11030411
DOID:9993 hypoglycemia HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0112262 leucine-sensitive hypoglycemia of infancy HGNC:59 Homo sapiens (human) 6833 ABCC8
  • RGD:7240710
DOID:2018 hyperinsulinism HGNC:59 Homo sapiens (human) 6833 ABCC8
  • PMID:12199344
DOID:11446 sciatic neuropathy HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:1824 status epilepticus HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0070219 familial hyperinsulinemic hypoglycemia 1 HGNC:59 Homo sapiens (human) 6833 ABCC8
  • RGD:7240710
DOID:11832 visual epilepsy HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:57 Homo sapiens (human) 368 ABCC6
  • PMID:12176944
DOID:2738 pseudoxanthoma elasticum HGNC:57 Homo sapiens (human) 368 ABCC6
  • MGI:6194238
  • PMID:10835643
  • PMID:11692167
  • PMID:12714611
  • PMID:15459974
  • PMID:16392638
  • PMID:16835894
  • PMID:17617515
  • RGD:7240710
DOID:0050644 arterial calcification of infancy HGNC:57 Homo sapiens (human) 368 ABCC6
  • MGI:6194238
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:56 Homo sapiens (human) 10057 ABCC5
  • PMID:15688370
DOID:13580 cholestasis HGNC:55 Homo sapiens (human) 10257 ABCC4
  • MGI:6194238
DOID:13619 extrahepatic cholestasis HGNC:55 Homo sapiens (human) 10257 ABCC4
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:55 Homo sapiens (human) 10257 ABCC4
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:54 Homo sapiens (human) 8714 ABCC3
  • PMID:15688370
DOID:557 kidney disease HGNC:54 Homo sapiens (human) 8714 ABCC3
  • MGI:6194238
DOID:783 end stage renal disease HGNC:54 Homo sapiens (human) 8714 ABCC3
  • MGI:6194238
DOID:12700 hyperprolactinemia HGNC:54 Homo sapiens (human) 8714 ABCC3
  • 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