HMGN1

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

Non-histone chromosomal protein HMG-14 is a protein that in humans is encoded by the HMGN1 gene.[5][6][7]

AliasesHMGN1, HMG14, high mobility group nucleosome binding domain 1
End39,349,647 bp[1]
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HMGN1
Identifiers
AliasesHMGN1, HMG14, high mobility group nucleosome binding domain 1
External IDsOMIM: 163920; MGI: 96120; HomoloGene: 3643; GeneCards: HMGN1; OMA:HMGN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004965

NM_008251

RefSeq (protein)

NP_004956

NP_032277

Location (UCSC)Chr 21: 39.34 – 39.35 MbChr 16: 95.92 – 95.93 Mb
PubMed search[3][4]
Wikidata
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Function

Chromosomal protein HMG14 and its close analog HMG17 (MIM 163910) bind to the inner side of the nucleosomal DNA, potentially altering the interaction between the DNA and the histone octamer. The 2 proteins may be involved in the process that maintains transcribable genes in a unique chromatin conformation.[8] Their ubiquitous distribution and relative abundance, as well as the high evolutionary conservation of the DNA-binding domain of the HMG14 family of proteins, suggest that they may be involved in an important cellular function.[7]

Interactions

HMGN1 has been shown to interact with YWHAZ.[9]

See also

References

Further reading

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