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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 October 9, 2024
Displaying entries 70551 - 70575 of 71927 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:1612 breast cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • RGD:7240710
DOID:2559 opiate dependence HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:219 colon cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:31932471
DOID:13482 Proteus syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:21793738
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:23632475
  • PMID:32276600
DOID:5199 ureteral obstruction HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:607 paraplegia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:1875 impotence HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:10763 hypertension HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:0050156 idiopathic pulmonary fibrosis HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:31874165
DOID:8552 chronic myeloid leukemia HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17900686
DOID:2526 prostate adenocarcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20638364
DOID:9352 type 2 diabetes mellitus HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17681738
DOID:7575 pancreatic intraductal papillary-mucinous neoplasm HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:24132918
DOID:8805 intermediate coronary syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20467748
DOID:3498 pancreatic ductal adenocarcinoma HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:19077459
DOID:10652 Alzheimer's disease HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:11597610
DOID:12858 Huntington's disease SGD:S000005560 Saccharomyces cerevisiae S288C 854199 AKR2
  • MGI:6194238
DOID:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:0111773 46,XY sex reversal 8 HGNC:387 Homo sapiens (human) 1109 AKR1C4
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
  • PMID:19681734

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024