NME1-NME2

NME1-NME2
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesNME1-NME2, NM23-LV, NMELV, NME1-NME2 readthrough
External IDsMGI: 3648428 HomoloGene: 39553 GeneCards: NME1-NME2
Gene location (Human)
Chr.Chromosome 17 (human)[1]
Band17q21.33Start51,153,590 bp[1]
End51,171,744 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

654364

433968

Ensembl

ENSG00000011052

n/a

UniProt

P22392

n/a

RefSeq (mRNA)

NM_001018136

n/a

RefSeq (protein)

NP_001018146

n/a

Location (UCSC)Chr 17: 51.15 – 51.17 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

NM23-LV, also known as NME1-NME2, is a human gene.[4]

The NME1-NME2 mRNA is a naturally occurring co-transcribed product of the neighboring NME1 and NME2 genes. The significance of this co-transcribed mRNA and the function of its predicted protein product have not yet been determined. Alternative splicing of this gene results in different transcript variants encoding distinct isoforms, but the full-length nature of each variant has not been defined.[4]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000011052 - Ensembl, May 2017
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. 1 2 "Entrez Gene: NME1-NME2 NM23-LV".

Further reading

  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Valentijn LJ, Koster J, Versteeg R (2006). "Read-through transcript from NM23-H1 into the neighboring NM23-H2 gene encodes a novel protein, NM23-LV". Genomics. 87 (4): 483–9. doi:10.1016/j.ygeno.2005.11.004. PMID 16442775.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.