HNF1A wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HNF1A wild-type allele is located in the vicinity of 12q24.31 and is approximately 25 kb in length. This allele, which encodes hepatocyte nuclear factor 1-alpha protein, is involved in both transcriptional regulation and DNA binding. Mutation of the gene is associated with familial hepatic adenoma, maturity-onset diabetes of the young type 3 and diabetes mellitus insulin-dependent type 20.

**Synonyms:** - Albumin Proximal Factor Gene - HNF-1-alpha - HNF-1A - HNF1 - HNF1 Homeobox A wt Allele - HNF1alpha - Hepatic Nuclear Factor 1 Gene - Hepatic Nuclear Factor-1-Alpha Gene - Hepatocyte Nuclear Factor 1 Alpha Gene - Hepatocyte Nuclear Factor 1 Gene - IDDM20 - Interferon Production Regulator Factor Gene - LF-B1, Hepatic Nuclear Factor (HNF1), Albumin Proximal Factor Gene - LFB1 - MODY3 - TCF-1 - TCF1 - Transcription Factor 1, Hepatic Gene - Transcription Factor 1, Hepatic; LF-B1, Hepatic Nuclear Factor (HNF1), Albumin Proximal Factor Gene