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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 6601 - 6625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
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:3770 pulmonary fibrosis HGNC:921 Homo sapiens (human) 27087 B3GAT1
  • MGI:6194238
DOID:9884 muscular dystrophy HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:16575835
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
DOID:9296 cleft lip HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:18640039
DOID:0050700 cardiomyopathy HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:22549409
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:1793 pancreatic cancer HGNC:920 Homo sapiens (human) 10317 B3GALT5
  • PMID:14555842
DOID:10652 Alzheimer's disease HGNC:92 Homo sapiens (human) 37 ACADVL
  • PMID:25260493
DOID:0080155 very long chain acyl-CoA dehydrogenase deficiency HGNC:92 Homo sapiens (human) 37 ACADVL
  • MGI:6194238
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:92 Homo sapiens (human) 37 ACADVL
  • MGI:6194238
DOID:10283 prostate cancer HGNC:9156 Homo sapiens (human) 5407 PNLIPRP1
  • PMID:11384102

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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