The role of HNF4A variants in the risk of type 2 diabetes

Curr Diab Rep. 2005 Apr;5(2):149-56. doi: 10.1007/s11892-005-0043-y.

Abstract

Genes influence susceptibility to type 2 diabetes mellitus (T2DM), and both positional cloning and candidate gene approaches have been used to identify these genes. Linkage analysis has generated evidence for T2DM-predisposing variants on chromosome 20q in studies of Caucasians, Asians, and Africans, and fine-mapping recently identified a likely susceptibility gene, hepatocyte nuclear factor 4-alpha (HNF4A). Rare loss-of-function mutations in HNF4A cause maturity-onset diabetes of the young and now common noncoding variants have been found to be associated with T2DM.

Publication types

  • Review

MeSH terms

  • DNA-Binding Proteins / genetics*
  • Diabetes Mellitus, Type 2 / epidemiology
  • Diabetes Mellitus, Type 2 / genetics*
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Hepatocyte Nuclear Factor 4
  • Humans
  • Mutation
  • Phosphoproteins / genetics*
  • Risk Assessment
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • Hepatocyte Nuclear Factor 4
  • Phosphoproteins
  • Transcription Factors