Aliases for HNF1A Gene
External Ids for HNF1A Gene
Previous HGNC Symbols for HNF1A Gene
Previous GeneCards Identifiers for HNF1A Gene
The protein encoded by this gene is a transcription factor required for the expression of several liver-specific genes. The encoded protein functions as a homodimer and binds to the inverted palindrome 5'-GTTAATNATTAAC-3'. Defects in this gene are a cause of maturity onset diabetes of the young type 3 (MODY3) and also can result in the appearance of hepatic adenomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]
GeneCards Summary for HNF1A Gene
HNF1A (HNF1 Homeobox A) is a Protein Coding gene. Diseases associated with HNF1A include diabetes mellitus, insulin-dependent, 20 and mody, type iii. Among its related pathways are FOXA2 and FOXA3 transcription factor networks and Type II diabetes mellitus. GO annotations related to this gene include transcription factor activity, sequence-specific DNA binding and sequence-specific DNA binding. An important paralog of this gene is HNF1B.
UniProtKB/Swiss-Prot for HNF1A Gene
Transcriptional activator that regulates the tissue specific expression of multiple genes, especially in pancreatic islet cells and in liver. Required for the expression of several liver specific genes. Binds to the inverted palindrome 5-GTTAATNATTAAC-3.