Skip to main content
. 2015 Dec 14;6:10232. doi: 10.1038/ncomms10232

Table 1. Frequencies of thalamocortical phenotypes in the compound mutants.

Genotype Normal n (%) Mild n (%) Severe n (%)
draxin−/− (n=8) 0 0 8 (100%)
draxin+/− (n=8) 8 (100%) 0 0
Dcc−/− (n=8) 8 (100%) 0 0
draxin+/−;Dcc+/− (n=11) 7 (64%) 4 (36%) 0
draxin+/−; Dcc−/− (n=8) 0 0 8 (100%)
Neo1Gt/Gt (n=8) 8 (100%) 0 0
draxin+/−;Neo1Gt/+ (n=9) 6 (67%) 3 (33%) 0
draxin+/−;Neo1Gt/Gt (n=8) 0 2 (25%) 6 (75%)
Unc5a−/− (n=8) 8 (100%) 0 0
draxin+/−;Unc5a+/− (n=8) 8 (100%) 0 0
draxin+/−;Unc5a−/− (n=8) 8 (100%) 0 0
Unc5b−/− (n=0) Embryonic lethal (E10)
draxin+/−;Unc5b+/− (n=8) 8 (100%) 0 0
Dscam−/− (n=8) 8 (100%) 0 0
draxin+/−;Dscam+/− (n=8) 8 (100%) 0 0
draxin+/−;Dscam−/− (n=8) 8 (100%) 0 0
Neo1Gt/Gt;Dcc−/− (n=6) 0 0 6 (100%)

draxin+/−;Dcc−/−, draxin+/−;Neo1Gt/Gt and Neo1Gt/Gt;Dcc−/− mice exhibited severe thalamocortical projection defects that resembled those in draxin−/− mice.