VSX2

(redirected from RET1)

VSX2

A gene on chromosome 14q24.3 that encodes a homeobox protein which plays a key role in the specification and morphogenesis of the sensory retina. It may participate in the development of the cells of the inner nuclear layer, particularly bipolar cells.

Molecular pathology
VSX2 mutations are associated with microphthalmia, cataracts and iris abnormalities.
References in periodicals archive ?
Thus, from this raw data, it cannot be concluded that that RDM has a strong positive relationship with RET1 since this relationship could be distorted by firm size.
69 volume Table 2 Correlations among stock return, volatility, and trading volume for Chinese stock markets (April 1991-June 1999) RET1 RET2 VOLA1 VOLA2 VOLUME1 VOLUME2 RET1 1.