This gene is a member of the large family ofconnexins that are required for the formation ofgap junctions. Six connexin monomers form a hemichannel, or connexon, on the cell surface. This connexon can interact with a connexon from a neighboring cell, thus forming a channel linking the cytoplasm of the 2 cells.[5]
White TW, Srinivas M, Ripps H, et al. (2002). "Virtual cloning, functional expression, and gating analysis of human connexin31.9".Am. J. Physiol., Cell Physiol.283 (3): C960–70.doi:10.1152/ajpcell.00163.2002.PMID12176752.
Belluardo N, White TW, Srinivas M, et al. (2001). "Identification and functional expression of HCx31.9, a novel gap junction gene".Cell Commun. Adhes.8 (4–6):173–8.doi:10.3109/15419060109080719.PMID12064584.S2CID13136344.
Söhl G, Nielsen PA, Eiberger J, Willecke K (2003). "Expression profiles of the novel human connexin genes hCx30.2, hCx40.1, and hCx62 differ from their putative mouse orthologues".Cell Commun. Adhes.10 (1):27–36.doi:10.1080/15419060302063.PMID12881038.S2CID225894.
Kreuzberg MM, Liebermann M, Segschneider S, et al. (2009). "Human connexin31.9, unlike its orthologous protein connexin30.2 in the mouse, is not detectable in the human cardiac conduction system".J. Mol. Cell. Cardiol.46 (4):553–9.doi:10.1016/j.yjmcc.2008.12.007.PMID19168070.
