NFYB

Information NFYB

Description

The protein encoded by this gene is one subunit of a trimeric complex, forming a highly conserved transcription factor that binds with high specificity to CCAAT motifs in the promoter regions in a variety of genes. This gene product, subunit B, forms a tight dimer with the C subunit, a prerequisite for subunit A association. The resulting trimer binds to DNA with high specificity and affinity. Subunits B and C each contain a histone-like motif. Observation of the histone nature of these subunits is supported by two types of evidence; protein sequence alignments and experiments with mutants. [provided by RefSeq, Jul 2008]

Full Name

nuclear transcription factor Y subunit beta

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
3
Peaks
45,612
Non-redundant peaks
24,956

TF Classification

Super Class
Other all-alpha-helical DNA-binding domains
Class
Heteromeric CCAAT-binding factors
Familly
Heteromeric CCAAT-binding factors
Sub Familly
None

Source TFClass

External IDs

JASPAR
MA0502
Ensembl
ENSG00000120837
UniProt
P25208
Genevisible
P25208
RefSeq
NM_006166
Aliases
CBF-A; CBF-B; HAP3; NF-YB
All peaks NFYB
Download BED file
Non redundant peaks NFYB
Download BED file
SEQUENCES NFYB
Download FASTA file
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Datasets Table for NFYB

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
NFYB GM12878 ENCODE Homo sapiens ENCSR000DNM 8,893
NFYB K-562 ENCODE Homo sapiens ENCSR000EGQ 13,231
NFYB HeLa-S3 ENCODE Homo sapiens ENCSR000DNR 8,235
NFYB K-562 GEO Homo sapiens GSE26439 15,253
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.