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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 5451 - 5475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5212 congenital disorder of glycosylation FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:2377 multiple sclerosis FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:2986 IgA glomerulonephritis FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:28 endocrine system disease FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:0060256 Dowling-Degos disease FB:FBgn0033901 Drosophila melanogaster (fruit fly) 36564 O-fut1 CG12366
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:6107 Homo sapiens (human) 3651 PDX1
  • PMID:18506375
DOID:9970 obesity HGNC:6107 Homo sapiens (human) 3651 PDX1
  • PMID:15979049
DOID:9744 type 1 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:0080998 acute necrotizing pancreatitis HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:3891 placental insufficiency HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:0111103 maturity-onset diabetes of the young type 4 HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:17131142
DOID:0050877 pancreatic agenesis HGNC:6107 Homo sapiens (human) 3651 PDX1
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:10545531
  • PMID:15170499
  • PMID:15734849
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:3534 Lafora disease RGD:735081 Rattus norvegicus (Norway rat) 364682 Nhlrc1
  • MGI:6194238
DOID:13359 Ehlers-Danlos syndrome RGD:1309214 Rattus norvegicus (Norway rat) 364675 B4galt7
  • MGI:6194238
DOID:0080738 Ehlers-Danlos syndrome spondylodysplastic type 1 RGD:1309214 Rattus norvegicus (Norway rat) 364675 B4galt7
  • MGI:6194238
DOID:10763 hypertension HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9970 obesity HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9352 type 2 diabetes mellitus HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:12086927
  • PMID:15220217
DOID:5408 Paget's disease of bone HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • 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