Homo sapiens Gene: HMGN4
Summary
InnateDB Gene IDBG-69608.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HMGN4
Gene Name high mobility group nucleosomal binding domain 4
Synonyms HMG17L3; NHC;
Species Homo sapiens
Ensembl Gene ENSG00000182952
Encoded Proteins
high mobility group nucleosomal binding domain 4
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 6:26538405-26546254
Strand Forward strand
Band p22.2
Transcripts
ENST00000377575 ENSP00000366798
ENST00000477243
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
Experimentally validated
Total 7 [view]
Protein-Protein 6 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0031492 nucleosomal DNA binding
Biological Process
Cellular Component
GO:0000785 chromatin
GO:0005634 nucleus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.236774
RefSeq NM_006353
HUGO
OMIM
CCDS CCDS4615
HPRD 17111
IMGT
EMBL
GenPept
RNA Seq Atlas