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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 8726 - 8750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8778 Crohn's disease FB:FBgn0026754 Drosophila melanogaster (fruit fly) 53583 Ugt37C1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0026754 Drosophila melanogaster (fruit fly) 53583 Ugt37C1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus FB:FBgn0026754 Drosophila melanogaster (fruit fly) 53583 Ugt37C1
  • MGI:6194238
DOID:1612 breast cancer FB:FBgn0026754 Drosophila melanogaster (fruit fly) 53583 Ugt37C1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0026755 Drosophila melanogaster (fruit fly) 53584 Ugt37B1
  • MGI:6194238
DOID:7998 hyperthyroidism FB:FBgn0026755 Drosophila melanogaster (fruit fly) 53584 Ugt37B1
  • MGI:6194238
DOID:3803 Crigler-Najjar syndrome FB:FBgn0026755 Drosophila melanogaster (fruit fly) 53584 Ugt37B1
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder FB:FBgn0026755 Drosophila melanogaster (fruit fly) 53584 Ugt37B1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus FB:FBgn0026755 Drosophila melanogaster (fruit fly) 53584 Ugt37B1
  • MGI:6194238
DOID:9675 pulmonary emphysema MGI:1858901 Mus musculus (house mouse) 53618 Fut8
  • PMID:16236725
DOID:1289 neurodegenerative disease HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:0090101 lethal congenital glycogen storage disease of heart HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:384 Wolff-Parkinson-White syndrome HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:0112002 immunodeficiency 47 HGNC:868 Homo sapiens (human) 537 ATP6AP1
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation HGNC:9115 Homo sapiens (human) 5373 PMM2
  • PMID:10066032
  • PMID:11058896
DOID:9970 obesity HGNC:9155 Homo sapiens (human) 5406 PNLIP
  • MGI:6194238
DOID:10283 prostate cancer HGNC:9156 Homo sapiens (human) 5407 PNLIPRP1
  • PMID:11384102
DOID:0080552 congenital disorder of glycosylation Ia MGI:1859214 Mus musculus (house mouse) 54128 Pmm2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation MGI:1859214 Mus musculus (house mouse) 54128 Pmm2
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:1859214 Mus musculus (house mouse) 54128 Pmm2
  • MGI:6194238
  • PMID:7884320
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type HGNC:19237 Homo sapiens (human) 54187 NANS
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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