- SOX14
SRY (sex determining region Y)-box 14, also known as SOX14, is a human
gene .cite web | title = Entrez Gene: SOX14 SRY (sex determining region Y)-box 14| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8403| accessdate = ]PBB_Summary
section_title =
summary_text = This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.cite web | title = Entrez Gene: SOX14 SRY (sex determining region Y)-box 14| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8403| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Wilson M, Koopman P |title=Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators. |journal=Curr. Opin. Genet. Dev. |volume=12 |issue= 4 |pages= 441–6 |year= 2003 |pmid= 12100890 |doi=
*cite journal | author=Schepers GE, Teasdale RD, Koopman P |title=Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families. |journal=Dev. Cell |volume=3 |issue= 2 |pages= 167–70 |year= 2002 |pmid= 12194848 |doi=
*cite journal | author=Cremazy F, Soullier S, Berta P, Jay P |title=Further complexity of the human SOX gene family revealed by the combined use of highly degenerate primers and nested PCR. |journal=FEBS Lett. |volume=438 |issue= 3 |pages= 311–4 |year= 1998 |pmid= 9827568 |doi=
*cite journal | author=Arsic N, Rajic T, Stanojcic S, "et al." |title=Characterisation and mapping of the human SOX14 gene. |journal=Cytogenet. Cell Genet. |volume=83 |issue= 1-2 |pages= 139–46 |year= 1999 |pmid= 9925951 |doi=
*cite journal | author=Malas S, Duthie S, Deloukas P, Episkopou V |title=The isolation and high-resolution chromosomal mapping of human SOX14 and SOX21; two members of the SOX gene family related to SOX1, SOX2, and SOX3. |journal=Mamm. Genome |volume=10 |issue= 9 |pages= 934–7 |year= 1999 |pmid= 10441749 |doi=
*cite journal | author=Wilmore HP, Smith MJ, Wilcox SA, "et al." |title=SOX14 is a candidate gene for limb defects associated with BPES and Möbius syndrome. |journal=Hum. Genet. |volume=106 |issue= 3 |pages= 269–76 |year= 2000 |pmid= 10798354 |doi=
*cite journal | author=Hargrave M, James K, Nield K, "et al." |title=Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases. |journal=Hum. Genet. |volume=106 |issue= 4 |pages= 432–9 |year= 2000 |pmid= 10830911 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504PBB_Controls
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