ReMap 2018 v1.2

An integrative ChIP-seq analysis of regulatory regions

Grhl2

Function : grainyhead like transcription factor 2
Description : The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]

Classification  

Super Class Immunoglobulin fold
Class Grainyhead domain factors
Family Grainyhead-related factors
Sub Family GRH-like proteins

External references

Ensembl ENSG00000083307
RefSeq NP_079191
Uniprot Q6ISB3
Aliases BOM, DFNA28, ECTDS, TFCP2L3
UCSC Gene coordinates chr8:101492439-101678104

External Links

JASPAR MA1105.1
Wikipedia Grhl2
WikiGenes Grhl2
Transcription Factor Encylopedia Grhl2    
GeneCards Grhl2
FactorBook Grhl2


Genomic visualization & Analyses for MACS

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for MACS

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

MACS - Datasets retained for Grhl2

Genomic visualization & Analyses for JAMM

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for JAMM

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

JAMM - Datasets retained for Grhl2