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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 10201 - 10225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9452 steatotic liver disease SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:9970 obesity SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:10584 retinitis pigmentosa SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw SGD:S000002990 Saccharomyces cerevisiae S288C 852862 STT3
  • MGI:6194238
  • PMID:34653363
DOID:0080573 congenital disorder of glycosylation Ix SGD:S000002990 Saccharomyces cerevisiae S288C 852862 STT3
  • MGI:6194238
DOID:0070254 congenital disorder of glycosylation type IIb SGD:S000002995 Saccharomyces cerevisiae S288C 852857 CWH41
  • MGI:6194238
DOID:0080470 developmental and epileptic encephalopathy 36 SGD:S000003015 Saccharomyces cerevisiae S288C 852835 ALG13
  • MGI:6194238
DOID:3651 pyruvate carboxylase deficiency disease SGD:S000003030 Saccharomyces cerevisiae S288C 852818 PYC1
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome SGD:S000003052 Saccharomyces cerevisiae S288C 852796 GUP1
  • MGI:6194238
DOID:10112 sleeping sickness SGD:S000003110 Saccharomyces cerevisiae S288C 852735 GPI10
  • PMID:10954751
DOID:0112216 developmental and epileptic encephalopathy 80 SGD:S000003110 Saccharomyces cerevisiae S288C 852735 GPI10
  • MGI:6194238
DOID:10584 retinitis pigmentosa SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:10763 hypertension SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:2018 hyperinsulinism SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:9452 steatotic liver disease SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:10923 sickle cell anemia SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:9993 hypoglycemia SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:11714 gestational diabetes SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:4194 glucose metabolism disease SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • 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