The targeting vector was designed with a human MIR125B1 cDNA inserted between 2 splicing sites in the 3' untranslated region of an EGFP sequence and followed by a polyA signal. The targeting vector was then used to replace the Cre ORF in a mutant embryonic stem cell line (see note) and placed under the control of the tet response promoter (TRE). The construct was inserted into a cassette exchange locus upstream of the Hprt gene using Inducible Cassette Exchange (ICE) recombination. (J:240427)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count