HOXB5

Information HOXB5

Description

This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in lung and gut development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML) and the occurrence of bronchopulmonary sequestration (BPS) and congenital cystic adenomatoid malformation (CCAM) tissue. [provided by RefSeq, Jul 2008]

Full Name

homeobox B5

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
7,315
Non-redundant peaks
7,315

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

NCBI Gene
3215
Official Gene Name
HOXB5
JASPAR
Ensembl
ENSG00000120075
UniProt
P09067
Genevisible
P09067
RefSeq
NM_002147
Aliases
HHO.C10; HOX2; HOX2A; HU-1; Hox2.1
All peaks HOXB5
Download BED file
Non redundant peaks HOXB5
Download BED file
SEQUENCES HOXB5
Download FASTA file
DOWNLOAD All ReMap
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Datasets Table for HOXB5

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
HOXB5 A-549 ENCODE Homo sapiens ENCSR748HJZ 7,315
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks