PTMS (gene)

Parathymosin is a protein that in humans is encoded by the PTMS gene.[3][4]

PTMS
Identifiers
AliasesPTMS, ParaT, parathymosin
External IDsOMIM: 168440 HomoloGene: 136762 GeneCards: PTMS
Gene location (Human)
Chr.Chromosome 12 (human)[1]
Band12p13.31Start6,765,516 bp[1]
End6,770,952 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

5763

n/a

Ensembl

ENSG00000159335

n/a

UniProt

P20962

n/a

RefSeq (mRNA)

NM_002824
NM_001330333

n/a

RefSeq (protein)

NP_001317262
NP_002815

n/a

Location (UCSC)Chr 12: 6.77 – 6.77 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human


References

  1. GRCh38: Ensembl release 89: ENSG00000159335 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Martic G, Karetsou Z, Kefala K, Politou AS, Clapier CR, Straub T, Papamarcaki T (Apr 2005). "Parathymosin affects the binding of linker histone H1 to nucleosomes and remodels chromatin structure". J Biol Chem. 280 (16): 16143–50. doi:10.1074/jbc.M410175200. PMID 15716277.
  4. "Entrez Gene: PTMS parathymosin".

Further reading


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