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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 1 - 25 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3908 lung non-small cell carcinoma HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:27777637
DOID:219 colon cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:1793 pancreatic cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:1324 lung cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:9352 type 2 diabetes mellitus HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • PMID:14764791
DOID:1440 Machado-Joseph disease HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
  • PMID:29867208
DOID:0050453 lissencephaly MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:0111237 congenital muscular dystrophy-dystroglycanopathy type A1 MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:9884 muscular dystrophy MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:0050700 cardiomyopathy MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:9296 cleft lip MGI:2138994 Mus musculus (house mouse) 99011 Pomt1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
DOID:0110184 Charcot-Marie-Tooth disease type 4J HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:0080923 bilateral parasagittal parieto-occipital polymicrogyria HGNC:16873 Homo sapiens (human) 9896 FIG4
  • RGD:7240710
DOID:0060589 Yunis-Varon syndrome HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:0060202 amyotrophic lateral sclerosis type 11 HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:10595 Charcot-Marie-Tooth disease HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
DOID:10024 migraine with aura MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:863 nervous system disease MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:0070384 developmental and epileptic encephalopathy 98 MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:0060178 familial hemiplegic migraine MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • 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