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Hnf1 homeobox a (hepatocyte nuclear factor 1 homeobox a), also known as hnf1a, is a human gene on chromosome 12 Google's service, offered free of charge, instantly translates words, phrases, and web pages between english and over 100 other languages. [5] [6] [7] it is ubiquitously expressed in many tissues and cell types

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Hnf1a (hnf1 homeobox a) is a protein coding gene Hnf1α is highly polymorphic, but lacks a mutation hot spot. Hepatic nuclear factor 1 alpha (hnf1a) hnf1a is a gene which acts as a switch that turns on and off other genes in the body

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Changes in the hnf1a gene cause diabetes by lowering the amount.

(2001) reported that mutations in the hnf1a gene have been identified in all racial and ethnic backgrounds, including european, chinese, japanese, african, and american indian. Hnf1a regulates the crosstalk between innate immune responses and mafld by mediating autophagic degradation of tbk1 A transcriptional regulatory network of hnf4alpha and. Hepatocyte nuclear factor 1 homeobox a (hnf1α) is widely expressed in pancreatic β cells, the liver, the intestines, and other organs

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