HNF1A
Information HNF1A
- Description
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]
- Full Name
HNF1 homeobox A
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 4
- Biotypes
- 3
- Peaks
- 48,042
- Non-redundant peaks
- 33,387
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
Datasets Table for HNF1A
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| HNF1A | Hep-G2 | ENCODE | Homo sapiens | ENCSR800QIT | 15,199 | |||
| HNF1A | NY15 | GEO | Homo sapiens | GSE108150 | 7,787 | |||
| HNF1A | HEE | 1 | GEO | Homo sapiens | GSE76376 | 15,543 | ||
| HNF1A | HEE | 5 | GEO | Homo sapiens | GSE76376 | 9,513 | ||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |