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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 3851 - 3875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • PMID:28096054
DOID:2749 glycogen storage disease Ia HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
  • PMID:11851840
  • PMID:20389290
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
  • PMID:10866049
DOID:9452 steatotic liver disease HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
DOID:14067 Plasmodium falciparum malaria HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24943486
DOID:9744 type 1 diabetes mellitus HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:15914531
DOID:5844 myocardial infarction HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:2383 neonatal jaundice HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24460025
DOID:557 kidney disease HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:12853069
DOID:13413 hepatic encephalopathy HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:1591 renovascular hypertension HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:6713 cerebrovascular disease HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:26072930
DOID:9281 phenylketonuria HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:12365 malaria HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24615128
  • PMID:25015414
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:35693827
DOID:13628 favism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • RGD:7240710
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766
DOID:0050328 congenital hypothyroidism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:13580 cholestasis HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24865682
DOID:583 hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:9279 hyperhomocysteinemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238

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International Collaboration

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