The use of pluripotentC-X-C chemokine receptor type 7 (CXCR-7) stem cells in regenerative medication and sickness modeling is complex by the variation in differentiation properties between lines. On this research, we characterized 13 human embryonic Rho inhibitor clinical trial stem cell (hESC) and 26 human induced pluripotent stem cell (hiPSC) lines to identify markers that predict neural differentiation habits. At a general degree, markers previously acknowledged to distinguish mouse ESCs from epiblast stem cells (EPI-SCs) correlated with neural differentiation conduct. Extra exclusively, quantitative analysis of miR-371-3 expression prospectively recognized hESC and hiPSC lines with differential neurogenic differentiation propensity and in vivo dopamine neuron engraftment likely. Transient KLF4 transduction greater miR-371-3 expression and altered neurogenic behavior and pluripotency marker expression. Conversely, suppression of miR-371-3 expression in KLF4-transduced cells rescued neural differentiation propensity. miR-371-3 expression degree as a result seems to have each a predictive in addition to a practical part in determining human pluripotent stem cell neurogenic differentiation conduct.