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HMGN2

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Protein-coding gene in the species Homo sapiens
HMGN2
Identifiers
AliasesHMGN2, HMG17, high mobility group nucleosomal binding domain 2
External IDsOMIM: 163910; HomoloGene: 136792; GeneCards: HMGN2; OMA:HMGN2 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)
Chromosome 1 (human)Genomic location for HMGN2Genomic location for HMGN2
Band1p36.11Start26,472,440 bp
End26,476,642 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • ventricular zone

  • ganglionic eminence

  • right uterine tube

  • Pituitary Gland

  • anterior pituitary

  • bone marrow cells

  • left ovary

  • thyroid gland

  • endometrium

  • right lobe of thyroid gland
    n/a
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
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 searchn/a
Wikidata
View/Edit Human

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

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000198830Ensembl, 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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