SOX14 References

SOX14
Identifiers
Aliases	SOX14, SOX28, SRY-box 14, SRY-box transcription factor 14
External IDs	OMIM: 604747 MGI: 98362 HomoloGene: 31224 GeneCards: SOX14
Gene location ( Human)
Chr.	Chromosome 3 (human)
End	137,766,334 bp
Gene location ( Mouse)
Chr.	Chromosome 9 (mouse)
End	99,758,223 bp
RNA expression pattern
	Top expressed in
	placenta; ; hypothalamus; ; substantia nigra; ; prostate; ; spinal cord;
	Top expressed in
	urethra; ; male urethra; ; mesencephalon; ; rhombencephalon; ; cerebellar cortex; ; hypothalamus; ; diencephalic nucleus; ; thalamus; ; list of thalamic nuclei; ; ureter;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	sequence-specific DNA binding; DNA binding; chromatin binding; protein binding; protein heterodimerization activity; DNA-binding transcription factor activity, RNA polymerase II-specific;
Cellular component	nucleus; cellular component;
Biological process	regulation of neuron migration; negative regulation of transcription, DNA-templated; regulation of transcription, DNA-templated; negative regulation of transcription by RNA polymerase II; transcription, DNA-templated; nervous system development; visual perception; entrainment of circadian clock; cell differentiation;
	Sources: Amigo / QuickGO
Orthologs
	8403
	20669
	ENSG00000168875
	ENSMUSG00000053747
	O95416
	Q04892
	NM_004189
	NM_011440
	NP_004180
	NP_035570
	Wikidata
View/Edit Human	View/Edit Mouse

Transcription factor SOX-14 is a protein that in humans is encoded by the SOX14 gene.^[5]^[6]

Function

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.^[6]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000168875 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000053747 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Arsic N, Rajic T, Stanojcic S, Goodfellow PN, Stevanovic M (Mar 1999). "Characterisation and mapping of the human SOX14 gene". Cytogenetics and Cell Genetics. 83 (1–2): 139–46. doi: 10.1159/000015149. PMID 9925951. S2CID 24812709.
^ ^a ^b "Entrez Gene: SOX14 SRY (sex determining region Y)-box 14".

Wilson M, Koopman P (August 2002). "Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators". Current Opinion in Genetics & Development. 12 (4): 441–6. doi: 10.1016/S0959-437X(02)00323-4. PMID 12100890.
Schepers GE, Teasdale RD, Koopman P (August 2002). "Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families". Developmental Cell. 3 (2): 167–70. doi: 10.1016/S1534-5807(02)00223-X. PMID 12194848.
Cremazy F, Soullier S, Berta P, Jay P (November 1998). "Further complexity of the human SOX gene family revealed by the combined use of highly degenerate primers and nested PCR". FEBS Letters. 438 (3): 311–4. doi: 10.1016/S0014-5793(98)01294-0. PMID 9827568. S2CID 551497.
Malas S, Duthie S, Deloukas P, Episkopou V (September 1999). "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". Mammalian Genome. 10 (9): 934–7. doi: 10.1007/s003359901118. PMID 10441749. S2CID 27862567.
Wilmore HP, Smith MJ, Wilcox SA, Bell KM, Sinclair AH (March 2000). "SOX14 is a candidate gene for limb defects associated with BPES and Möbius syndrome". Human Genetics. 106 (3): 269–76. doi: 10.1007/s004390051037. PMID 10798354.
Hargrave M, James K, Nield K, Toomes C, Georgas K, Sullivan T, Verzijl HT, Oley CA, Little M, De Jonghe P, Kwon JM, Kremer H, Dixon MJ, Timmerman V, Yamada T, Koopman P (April 2000). "Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases". Human Genetics. 106 (4): 432–9. doi: 10.1007/s004390000266. PMID 10830911. S2CID 20519444.

This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000168875 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000053747 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid9925951-5] Arsic N, Rajic T, Stanojcic S, Goodfellow PN, Stevanovic M (Mar 1999). "Characterisation and mapping of the human SOX14 gene". Cytogenetics and Cell Genetics. 83 (1–2): 139–46. doi: 10.1159/000015149. PMID 9925951. S2CID 24812709.

[entrez-6] "Entrez Gene: SOX14 SRY (sex determining region Y)-box 14".

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Function

References

Further reading