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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 3801 - 3825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0080573 congenital disorder of glycosylation Ix RGD:1311563 Rattus norvegicus (Norway rat) 363160 Stt3b
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix MGI:1915542 Mus musculus (house mouse) 68292 Stt3b
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw RGD:1311563 Rattus norvegicus (Norway rat) 363160 Stt3b
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw RGD:1565793 Rattus norvegicus (Norway rat) 500972 Stt3a
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw MGI:105124 Mus musculus (house mouse) 16430 Stt3a
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw FB:FBgn0011336 Drosophila melanogaster (fruit fly) 43005 Stt3B CG7748
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix FB:FBgn0011336 Drosophila melanogaster (fruit fly) 43005 Stt3B CG7748
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw FB:FBgn0031149 Drosophila melanogaster (fruit fly) 33082 Stt3A CG1518
  • MGI:6194238
DOID:0050589 inflammatory bowel disease RGD:1562048 Rattus norvegicus (Norway rat) 287920 St6galnac1
  • MGI:6194238
DOID:0050589 inflammatory bowel disease MGI:1341826 Mus musculus (house mouse) 20445 St6galnac1
  • PMID:35303419
DOID:3070 high grade glioma RGD:3676 Rattus norvegicus (Norway rat) 25197 St6gal1
  • PMID:11559557
DOID:3070 high grade glioma MGI:108470 Mus musculus (house mouse) 20440 St6gal1
  • MGI:6194238
DOID:1574 alcohol use disorder MGI:108470 Mus musculus (house mouse) 20440 St6gal1
  • MGI:6194238
DOID:1574 alcohol use disorder RGD:3676 Rattus norvegicus (Norway rat) 25197 St6gal1
  • MGI:6194238
DOID:0060470 salt and pepper syndrome RGD:620875 Rattus norvegicus (Norway rat) 83505 St3gal5
  • MGI:6194238
DOID:0060470 salt and pepper syndrome MGI:1339963 Mus musculus (house mouse) 20454 St3gal5
  • MGI:6194238
DOID:0080414 developmental and epileptic encephalopathy 15 MGI:1316659 Mus musculus (house mouse) 20441 St3gal3
  • MGI:6194238
DOID:0081180 autosomal recessive intellectual developmental disorder 12 RGD:68414 Rattus norvegicus (Norway rat) 64445 St3gal3
  • MGI:6194238
DOID:0081180 autosomal recessive intellectual developmental disorder 12 MGI:1316659 Mus musculus (house mouse) 20441 St3gal3
  • MGI:6194238
DOID:0080414 developmental and epileptic encephalopathy 15 RGD:68414 Rattus norvegicus (Norway rat) 64445 St3gal3
  • MGI:6194238
DOID:0070311 oligoasthenoteratozoospermia MGI:2183449 Mus musculus (house mouse) 217116 Spata20
  • PMID:29247744
DOID:0070311 oligoasthenoteratozoospermia RGD:735087 Rattus norvegicus (Norway rat) 360604 Spata20
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 RGD:3734 Rattus norvegicus (Norway rat) 24788 Sord
  • MGI:6194238
DOID:83 cataract RGD:3734 Rattus norvegicus (Norway rat) 24788 Sord
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy MGI:98266 Mus musculus (house mouse) 20322 Sord
  • 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