HMGN2

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
HMGN2
Identifiers
AliasesHMGN2, HMG17, high mobility group nucleosomal binding domain 2
External IDsHomoloGene: 136792 GeneCards: HMGN2
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for HMGN2
Genomic location for HMGN2
Band1p36.11Start26,472,450 bp[1]
End26,475,972 bp[1]
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]


References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000198830 - Ensembl, May 2017
  2. ^ "Human PubMed Reference:".
  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[edit]