(POU Domain, Class 4, Transcription Factor 3 (POU4F3))
This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009].
Chen, Johnson, Marcotti, Andrews, Moore, Rivolta: "Human fetal auditory stem cells can be expanded in vitro and differentiate into functional auditory neurons and hair cell-like cells." in: Stem cells (Dayton, Ohio), Vol. 27, Issue 5, pp. 1196-204, (2009) (PubMed).
van Drunen, Pauw, Collin, Kremer, Huygen, Cremers: "Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3." in: Audiology & neuro-otology, Vol. 14, Issue 5, pp. 303-7, (2009) (PubMed).
Aliases for POU4F3 抗体
POU class 4 homeobox 3 (POU4F3) 抗体 POU class 4 homeobox 3 (Pou4f3) 抗体 POU class 4 homeobox 3 (pou4f3) 抗体 POU domain, class 4, transcription factor 3 (Pou4f3) 抗体 BRN-3 抗体 BRN-3.1 抗体 brn-3c 抗体 BRN3 抗体 brn3.1 抗体 Brn3.1 抗体 BRN3C 抗体 brn3c 抗体 Brn3c 抗体 ddl 抗体 DFNA15 抗体 dreidel 抗体 POU4F3 抗体