HNF4A
Sign in to saveAlso known as HNF4, HNF4a7, HNF4a8, HNF4a9, HNF4alpha, MODY, MODY1, NR2A1
protein-coding gene in the species Homo sapiens
Gene data
HNF4A- Name
- hepatocyte nuclear factor 4 alpha
- Type
- protein-coding
- Position
- 44,355,439–44,432,845 (+)
- Aliases
- FRTS4, HNF4, HNF4a7, HNF4a8, HNF4a9, HNF4alpha, MODY, MODY1, NR2A1, NR2A21
- Ensembl
- ENSG00000101076
- RefSeq RNA
- NM_000457.6, NM_001030003.3, NM_001030004.3, NM_001258355.2, NM_001287182.2
- RefSeq protein
- NP_000448.3, NP_001025174.1, NP_001025175.1, NP_001245284.1, NP_001274111.1
The protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012].
Gene Ontology
Biological process
Molecular function
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
hepatocyte nuclear factor 4 alpha
- Symbol
- HNF4A
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 20:44,355,439-44,432,845
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein HNF4A PDB 1m7w.png
Show 7 more facts
- HomoloGene ID
- 395
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/3172
- genomic start
- 42984340
- chromosome
- human chromosome 20
- genomic end
- 44432845
- cytogenetic location
- 20q13.12
via Wikidata · CC0