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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 11926 - 11950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0060256 Dowling-Degos disease FB:FBgn0086253 Drosophila melanogaster (fruit fly) 326122 rumi CG31152
  • MGI:6194238
DOID:0080762 autosomal recessive limb-girdle muscular dystrophy type 2Z FB:FBgn0086253 Drosophila melanogaster (fruit fly) 326122 rumi CG31152
  • MGI:6194238
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy FB:FBgn0086253 Drosophila melanogaster (fruit fly) 326122 rumi CG31152
  • PMID:27807076
DOID:0111239 congenital muscular dystrophy-dystroglycanopathy type A10 Xenbase:XB-GENE-1009102 Xenopus tropicalis (tropical clawed frog) 100145540 rxylt1
  • MGI:6194238
DOID:0111239 congenital muscular dystrophy-dystroglycanopathy type A10 ZFIN:ZDB-GENE-060929-1018 Danio rerio (zebrafish) 557187 rxylt1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome ZFIN:ZDB-GENE-060929-1018 Danio rerio (zebrafish) 557187 rxylt1
  • PMID:27130732
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1009102 Xenopus tropicalis (tropical clawed frog) 100145540 rxylt1
  • MGI:6194238
DOID:0111239 congenital muscular dystrophy-dystroglycanopathy type A10 Xenbase:XB-GENE-1009106 Xenopus laevis (African clawed frog) 446820 rxylt1.S
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis ZFIN:ZDB-GENE-040219-1 Danio rerio (zebrafish) 403143 sarm1
  • MGI:6194238
DOID:1289 neurodegenerative disease ZFIN:ZDB-GENE-040219-1 Danio rerio (zebrafish) 403143 sarm1
  • MGI:6194238
DOID:10652 Alzheimer's disease FB:FBgn0086348 Drosophila melanogaster (fruit fly) 38973 se
  • MGI:6194238
DOID:14330 Parkinson's disease FB:FBgn0086348 Drosophila melanogaster (fruit fly) 38973 se
  • MGI:6194238
DOID:2841 asthma FB:FBgn0086348 Drosophila melanogaster (fruit fly) 38973 se
  • MGI:6194238
DOID:1059 intellectual disability FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • PMID:25125150
DOID:12716 newborn respiratory distress syndrome FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • MGI:6194238
DOID:14227 azoospermia FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • PMID:25361961
DOID:11198 DiGeorge syndrome FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • MGI:6194238
DOID:0060041 autism spectrum disorder FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • PMID:31316544
DOID:3827 congenital diaphragmatic hernia FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • MGI:6194238
DOID:0081210 autosomal recessive intellectual developmental disorder 46 FB:FBgn0020251 Drosophila melanogaster (fruit fly) 38736 sfl CG8339
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238
DOID:2871 endometrial carcinoma FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238
DOID:1824 status epilepticus FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238
DOID:0080855 Parkinsonism FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238
DOID:114 heart disease FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238

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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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