MNX1
Information MNX1
- Description
This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
- Full Name
motor neuron and pancreas homeobox 1
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 1
- Biotypes
- 1
- Peaks
- 49,482
- Non-redundant peaks
- 49,482
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 3110
- Official Gene Name
- MNX1
- JASPAR
- MA0707
- Ensembl
- ENSG00000130675
- UniProt
- P50219
- Genevisible
- P50219
- RefSeq
- NM_001165255
- Aliases
- HB9; HLXB9; HOXHB9; SCRA1
Datasets Table for MNX1
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| MNX1 | Hep-G2 | ENCODE | Homo sapiens | ENCSR108MKR | 49,482 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |