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HMGN2

From Wikipedia, the free encyclopedia

HMGN2
Identifiers
AliasesHMGN2, HMG17, high mobility group nucleosomal binding domain 2
External IDsOMIM: 163910; HomoloGene: 136792; GeneCards: HMGN2; OMA:HMGN2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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

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

See also

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References

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  1. 1 2 3 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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