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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 5601 - 5625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K HGNC:9202 Homo sapiens (human) 10585 POMT1
  • RGD:7240710
DOID:0050453 lissencephaly HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:17559086
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • PMID:12369018
  • PMID:15637732
  • PMID:16575835
DOID:0111237 congenital muscular dystrophy-dystroglycanopathy type A1 HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • RGD:7240710
DOID:3770 pulmonary fibrosis HGNC:921 Homo sapiens (human) 27087 B3GAT1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:922 Homo sapiens (human) 135152 B3GAT2
  • PMID:20950796
DOID:9206 Barrett's esophagus HGNC:922 Homo sapiens (human) 135152 B3GAT2
  • PMID:26545406
DOID:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
DOID:10908 hydrocephalus HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
  • PMID:16393287
DOID:5419 schizophrenia HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:10828087
DOID:5844 myocardial infarction HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:18549840
DOID:10763 hypertension HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:9427 hypertensive encephalopathy HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:12351 alcoholic hepatitis HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
  • PMID:19119483
DOID:9970 obesity HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:824 periodontitis HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:12938026
  • PMID:17850927
DOID:3393 coronary artery disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16043164
DOID:1485 cystic fibrosis HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16875506
DOID:1793 pancreatic cancer HGNC:9235 Homo sapiens (human) 5467 PPARD
  • PMID:17652168
DOID:4607 biliary tract cancer HGNC:9235 Homo sapiens (human) 5467 PPARD
  • PMID:18497548

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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