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              |  |   Gene Symbol   |  FOXA2  |  
              |  |  Aliases | 
                  HNF3B, TCF3B                 |  
              |  |  Entrez Gene ID   |  |  
              |  |  Gene Name  | 
                    Forkhead box A2                   |  
              |  |  Chromosomal Location | 
                      20p11.21                     |  
              |  |  HGNC ID |  |  
              |  |  Summary  | 
                      This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific genes such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. This gene has been linked to sporadic cases of maturity-onset diabetes of the young. Transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008] 
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              |  | e!Ensembl |  
              
                | Protein Information |  
                |  |  Protein Name |  Hepatocyte nuclear factor 3-beta, HNF-3-beta, HNF-3B, TCF-3B, forkhead box protein A2, hepatic nuclear factor-3-beta, transcription factor 3B  |  
              |  |  Function  |  |  
              |  |    UniProt |  |  
              |  |  PDB |  |  |  |  |  
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        | Interactions |  
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                | STRING | MINT | IntAct |  
                | ENSP00000394071 | P31150 | P31150 |  |  
      |  |  | View interactions |  
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      |    Associated Diseases  
        
| Disease group | Disease Name | References |  
      | Endocrine System Diseases |  
      | PCOS |  |  |  
      |  References  |  
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            |  Corton Marta,  Botella-Carretero Jose I,  Benguria Alberto,  Villuendas Gemma,  Zaballos Angel,  San Millan Jose L,  Escobar-Morreale Hector F,  Peral Belen  |  
            |  Instituto de Investigaciones Biomedicas, Consejo Superior de Investigaciones  Cientificas and Universidad Autonoma de Madrid, E-28029 Madrid, Spain.  |  
            |  J Clin Endocrinol Metab. 2007 Jan;92(1):328-37. doi: 10.1210/jc.2006-1665. Epub  |  
            | 
                 Abstract  
              CONTEXT: The polycystic ovary syndrome (PCOS) is frequently associated with  visceral obesity, suggesting that omental adipose tissue might play an important   role in the pathogenesis of the syndrome.  OBJECTIVE:  The objective was to study  the expression profiles of omental fat biopsy samples obtained from morbidly  obese women with or without PCOS at the time of bariatric surgery. DESIGN: This  was a case-control study. SETTINGS: We conducted the study in an academic  hospital. PATIENTS: Eight PCOS patients and seven nonhyperandrogenic women  submitted to bariatric surgery because of morbid obesity. INTERVENTIONS: Biopsy  samples of omental fat were obtained during bariatric surgery. MAIN OUTCOME  MEASURE: The main outcome measure was high-density oligonucleotide arrays.   RESULTS:  After statistical analysis, we identified changes in the expression  patterns of 63 genes between PCOS and control samples. Gene classification was  assessed through data mining of Gene Ontology annotations and cluster analysis of  dysregulated genes between both groups. These methods highlighted abnormal  expression of genes encoding certain components of several biological pathways  related to insulin signaling and Wnt signaling, oxidative stress, inflammation,  immune function, and lipid metabolism, as well as other genes previously related   to PCOS or to the metabolic syndrome. CONCLUSION: The differences in the gene  expression profiles in visceral adipose tissue of PCOS patients compared with  nonhyperandrogenic women involve multiple genes related to several biological  pathways, suggesting that the involvement of abdominal obesity in the  pathogenesis of PCOS is more ample than previously thought and is not restricted   to the induction of insulin resistance.  |  |  |  |  
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