SOX2OT

Last updated
SOX2-OT
Identifiers
Aliases SOX2-OT , NCRNA00043, SOX2 overlapping transcript
External IDs OMIM: 616338 GeneCards: SOX2-OT
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

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Location (UCSC)n/an/a
PubMed search [1] n/a
Wikidata
View/Edit Human

SOX2 overlapping transcript (SOX2OT) is a long non-coding RNA, containing at least 5 exons. The SOX2 gene, an important regulator of neurogenesis, lies within one of the introns of SOX2OT. [2] SOX2OT and SOX2DOT (an isoform of SOXOT transcribed from a distal highly conserved element) are expressed in zones of neurogenesis within the brain. It is associated with central nervous system structures in zebrafish and chicken embryonic brains, and is dynamically regulated during embryogenesis. [3] SOX2OT may play a role in vertebrate development. [3]

Contents

See also

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References

  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. Fantes J, Ragge NK, Lynch SA, et al. (April 2003). "Mutations in SOX2 cause anophthalmia". Nat. Genet. 33 (4): 461–3. doi: 10.1038/ng1120 . PMID   12612584.
  3. 1 2 Amaral PP, Neyt C, Wilkins SJ, et al. (November 2009). "Complex architecture and regulated expression of the Sox2ot locus during vertebrate development". RNA. 15 (11): 2013–27. doi:10.1261/rna.1705309. PMC   2764477 . PMID   19767420.

Further reading