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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 6751 - 6775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 SGD:S000005848 Saccharomyces cerevisiae S288C 854499 PMT3
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0111237 congenital muscular dystrophy-dystroglycanopathy type A1 SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
  • PMID:27358400
DOID:0112374 muscular dystrophy-dystroglycanopathy SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0050453 lissencephaly SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0050700 cardiomyopathy SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:9884 muscular dystrophy SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:9296 cleft lip SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:9884 muscular dystrophy SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0050453 lissencephaly SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0110298 autosomal recessive limb-girdle muscular dystrophy type 2N SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0112380 muscular dystrophy-dystroglycanopathy type B2 SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
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:653 purine-pyrimidine metabolic disorder HGNC:7892 Homo sapiens (human) 4860 PNP
  • PMID:3029074
DOID:5813 purine nucleoside phosphorylase deficiency HGNC:7892 Homo sapiens (human) 4860 PNP
  • MGI:6194238
  • RGD:7240710
DOID:5813 purine nucleoside phosphorylase deficiency SGD:S000004199 Saccharomyces cerevisiae S288C 850906 PNP1
  • MGI:6194238
DOID:653 purine-pyrimidine metabolic disorder SGD:S000004199 Saccharomyces cerevisiae S288C 850906 PNP1
  • MGI:6194238
DOID:9970 obesity HGNC:30802 Homo sapiens (human) 57104 PNPLA2
  • 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