HMGN2

Non-histone chromosomal protein HMG-17 is a protein that in humans is encoded by the HMGN2 gene.[3][4]

HMGN2
Identifiers
AliasesHMGN2, HMG17, high mobility group nucleosomal binding domain 2
External IDsOMIM: 163910 HomoloGene: 136792 GeneCards: HMGN2
Gene location (Human)
Chr.Chromosome 1 (human)[1]
Band1p36.11Start26,472,440 bp[1]
End26,476,642 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

3151

n/a

Ensembl

ENSG00000198830

n/a

UniProt

P05204

n/a

RefSeq (mRNA)

NM_005517

n/a

RefSeq (protein)

NP_005508

n/a

Location (UCSC)Chr 1: 26.47 – 26.48 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000198830 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Dracopoli NC, O'Connell P, Elsner TI, Lalouel JM, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, et al. (Jul 1991). "The CEPH consortium linkage map of human chromosome 1". Genomics. 9 (4): 686–700. doi:10.1016/0888-7543(91)90362-I. PMID 2037294.
  4. "Entrez Gene: HMGN2 high-mobility group nucleosomal binding domain 2".

Further reading

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