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HMGN3

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Protein-coding gene in the species Homo sapiens
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
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)
Chromosome 6 (human)Genomic location for HMGN3Genomic location for HMGN3
Band6q14.1Start79,201,245 bp
End79,234,738 bp
Gene location (Mouse)
Chromosome 9 (mouse)
Chr.Chromosome 9 (mouse)
Chromosome 9 (mouse)Genomic location for HMGN3Genomic location for HMGN3
Band9|9 E2Start82,992,001 bp
End83,028,738 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • bronchial epithelial cell

  • endothelial cell

  • palpebral conjunctiva

  • right uterine tube

  • parietal pleura

  • ventricular zone

  • mucosa of paranasal sinus

  • visceral pleura

  • hair follicle

  • germinal epithelium
Top expressed in
  • lens

  • conjunctival fornix

  • ciliary body

  • epithelium of lens

  • saccule

  • islet of Langerhans

  • condyle

  • olfactory epithelium

  • fossa

  • ventricular zone
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9324

94353

Ensembl

ENSG00000118418

ENSMUSG00000066456

UniProt

Q15651

Q9DCB1

RefSeq (mRNA)
NM_001201362
NM_001201363
NM_004242
NM_138730
NM_001318884

NM_001318885
NM_001318886
NM_001318887
NM_001318888

NM_026122
NM_175074

RefSeq (protein)
NP_001188291
NP_001188292
NP_001305813
NP_001305814
NP_001305815

NP_001305816
NP_001305817
NP_004233
NP_620058

NP_080398
NP_778249

Location (UCSC)Chr 6: 79.2 – 79.23 MbChr 9: 82.99 – 83.03 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000118418Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000066456Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Lee JW, Choi HS, Gyuris J, Brent R, Moore DD (Jul 1995). "Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor". Mol Endocrinol. 9 (2): 243–54. doi:10.1210/mend.9.2.7776974. PMID 7776974.
  6. West KL, Ito Y, Birger Y, Postnikov Y, Shirakawa H, Bustin M (Jul 2001). "HMGN3a and HMGN3b, two protein isoforms with a tissue-specific expression pattern, expand the cellular repertoire of nucleosome-binding proteins". J Biol Chem. 276 (28): 25959–69. doi:10.1074/jbc.M101692200. PMID 11356838.
  7. ^ "Entrez Gene: HMGN3 high mobility group nucleosomal binding domain 3".

Further reading

External links


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