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Protein-coding gene in the species Homo sapiens

HMGN3

HMGN3
All data from the card 17
Aliases
HMGN3, PNAS-25, TRIP7, PNAS-24, high mobility group nucleosomal binding domain 3
External IDs
OMIM: 604502; MGI: 2138069; GeneCards: HMGN3
Chr.
Chromosome 6 (human)
Band
6q14.1
End
79,234,738 bp
Chr.
Chromosome 9 (mouse)
Band
9|9 E2
End
83,028,738 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
9324
Ensembl
ENSG00000118418
UniProt
Q15651
RefSeq (mRNA)
NM_001201362NM_001201363NM_004242NM_138730NM_001318884NM_001318885NM_001318886NM_001318887NM_001318888
RefSeq (protein)
NP_001188291NP_001188292NP_001305813NP_001305814NP_001305815NP_001305816NP_001305817NP_004233NP_620058
Location (UCSC)
Chr 6: 79.2 – 79.23 Mb

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

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.

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Text from Wikipedia, CC BY-SA 4.0 · Source article