HMGN4

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

High mobility group nucleosome-binding domain-containing protein 4 is a transcription factor that in humans is encoded by the HMGN4 gene.[3][4]

AliasesHMGN4, HMG17L3, NHC, high mobility group nucleosomal binding domain 4
End26,546,933 bp[1]
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HMGN4
Identifiers
AliasesHMGN4, HMG17L3, NHC, high mobility group nucleosomal binding domain 4
External IDsHomoloGene: 105484; GeneCards: HMGN4; OMA:HMGN4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006353

n/a

RefSeq (protein)

NP_006344
NP_006344.1

n/a

Location (UCSC)Chr 6: 26.54 – 26.55 Mbn/a
PubMed search[2]n/a
Wikidata
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Function

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. Transcript variants utilizing alternative polyadenylation signals exist for this gene.[3]

See also

References

Further reading

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