HMGN3

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

High mobility group nucleosome-binding domain-containing protein 3 is a protein that in humans is encoded by the HMGN3 gene.[5][6][7]

AliasesHMGN3, PNAS-25, TRIP7, PNAS-24, high mobility group nucleosomal binding domain 3
End79,234,738 bp[1]
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HMGN3
Identifiers
AliasesHMGN3, PNAS-25, TRIP7, PNAS-24, high mobility group nucleosomal binding domain 3
External IDsOMIM: 604502; MGI: 2138069; HomoloGene: 130417; GeneCards: HMGN3; OMA:HMGN3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_026122
NM_175074

RefSeq (protein)

NP_080398
NP_778249

Location (UCSC)Chr 6: 79.2 – 79.23 MbChr 9: 82.99 – 83.03 Mb
PubMed search[3][4]
Wikidata
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Thyroid hormone receptors are hormone-dependent transcription factors that regulate expression of a variety of specific target genes. The protein encoded by this gene binds thyroid hormone receptor beta, but only in the presence of thyroid hormone. The encoded protein, 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. Two transcript variants encoding different isoforms have been found for this gene.[7]

References

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