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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 9926 - 9950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050560 Walker-Warburg syndrome SGD:S000000021 Saccharomyces cerevisiae S288C 851210 PMT2
  • MGI:6194238
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 SGD:S000000021 Saccharomyces cerevisiae S288C 851210 PMT2
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy SGD:S000000021 Saccharomyces cerevisiae S288C 851210 PMT2
  • MGI:6194238
DOID:0014667 disease of metabolism SGD:S000000036 Saccharomyces cerevisiae S288C 851193 CDC19
  • MGI:6194238
DOID:4195 hyperglycemia SGD:S000000036 Saccharomyces cerevisiae S288C 851193 CDC19
  • MGI:6194238
DOID:10763 hypertension SGD:S000000036 Saccharomyces cerevisiae S288C 851193 CDC19
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease SGD:S000000036 Saccharomyces cerevisiae S288C 851193 CDC19
  • MGI:6194238
DOID:0080566 congenital disorder of glycosylation In SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • PMID:18313027
DOID:162 cancer SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • PMID:26354769
DOID:0080556 congenital disorder of glycosylation Id SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3
  • MGI:6194238
  • PMID:23038983
DOID:5212 congenital disorder of glycosylation SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3
  • PMID:10581255
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 SGD:S000000208 Saccharomyces cerevisiae S288C 852289 GPI18
  • MGI:6194238
DOID:9870 galactosemia SGD:S000000222 Saccharomyces cerevisiae S288C 852306 GAL7
  • MGI:6194238
  • PMID:10799308
  • PMID:24077966
  • PMID:28213126
  • PMID:8794735
DOID:0111459 classic galactosemia SGD:S000000222 Saccharomyces cerevisiae S288C 852306 GAL7
  • MGI:6194238
DOID:0111458 galactose epimerase deficiency SGD:S000000223 Saccharomyces cerevisiae S288C 852307 GAL10
  • MGI:6194238
DOID:9870 galactosemia SGD:S000000223 Saccharomyces cerevisiae S288C 852307 GAL10
  • MGI:6194238
  • PMID:18188677
  • PMID:22613355
DOID:1588 thrombocytopenia SGD:S000000223 Saccharomyces cerevisiae S288C 852307 GAL10
  • PMID:30247636
DOID:162 cancer SGD:S000000233 Saccharomyces cerevisiae S288C 852317 CDS1
  • PMID:26354769
DOID:1168 familial hyperlipidemia SGD:S000000257 Saccharomyces cerevisiae S288C 852342 YBR053C
  • MGI:6194238
DOID:684 hepatocellular carcinoma SGD:S000000257 Saccharomyces cerevisiae S288C 852342 YBR053C
  • MGI:6194238
DOID:10534 stomach cancer SGD:S000000257 Saccharomyces cerevisiae S288C 852342 YBR053C
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 SGD:S000000274 Saccharomyces cerevisiae S288C 852362 ALG14
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1
  • PMID:24157261
DOID:0080563 congenital disorder of glycosylation Ik SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1
  • MGI:6194238
  • PMID:26931382

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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