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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 3776 - 3800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:11595724
  • PMID:20697673
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17681738
DOID:1245 vulva cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:22685591
DOID:0050156 idiopathic pulmonary fibrosis HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:31874165
DOID:162 cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:607 paraplegia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:3008 invasive ductal carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:18392055
DOID:9352 type 2 diabetes mellitus HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:13482 Proteus syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:21793738
  • RGD:7240710
DOID:2316 brain ischemia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:14745448
  • PMID:17825267
  • PMID:20214684
  • PMID:20921115
  • PMID:21049487
DOID:5844 myocardial infarction HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:20467748
DOID:14330 Parkinson's disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:18395980
  • PMID:19800394
  • PMID:21741444
DOID:8552 chronic myeloid leukemia HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17900686
DOID:8805 intermediate coronary syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20467748
DOID:2957 pulmonary tuberculosis HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20141546
DOID:3312 bipolar disorder HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20214684
DOID:326 ischemia HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:2526 prostate adenocarcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:20638364
DOID:0112263 hypoinsulinemic hypoglycemia with hemihypertrophy HGNC:392 Homo sapiens (human) 208 AKT2
  • RGD:7240710
DOID:3070 high grade glioma HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:19330838
DOID:10286 prostate carcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:24838891
DOID:162 cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238

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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