PHOX2B

Information PHOX2B

Description

The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription factor involved in the development of several major noradrenergic neuron populations and the determination of neurotransmitter phenotype. The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase, c-fos promoters and several enhancers, including cyclic amp-response element and serum-response element. Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome. [provided by RefSeq, Jul 2016]

Full Name

paired like homeobox 2B

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
2
Biotypes
2
Peaks
143,305
Non-redundant peaks
112,700

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

NCBI Gene
8929
Official Gene Name
PHOX2B
JASPAR
Ensembl
ENSG00000109132
UniProt
Q99453
Genevisible
Q99453
RefSeq
NM_003924
Aliases
CCHS; NBLST2; NBPhox; PMX2B; Phox2b
All peaks PHOX2B
Download BED file
Non redundant peaks PHOX2B
Download BED file
SEQUENCES PHOX2B
Download FASTA file
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Datasets Table for PHOX2B

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
PHOX2B CLB-Ga GEO Homo sapiens GSE90683 71,479
PHOX2B SK-N-BE2-C GEO Homo sapiens GSE94822 71,826
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks