Foxg1tm1.1(cre)Ddmo/Foxg1+ Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1a(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N
|
telencephalon hypoplasia |
J:335489
|
Foxg1tm1.1(cre)Ddmo/Foxg1+ Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1c(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N
|
telencephalon hypoplasia |
J:335489
|
Foxg1tm1.1(cre)Ddmo/Foxg1+ Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1d(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N
|
telencephalon hypoplasia |
J:335489
|
Foxg1tm1.1(cre)Ddmo/0 Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N
|
telencephalon hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1a(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Mef2c-cre)2Blk/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
abnormal heart right ventricle outflow tract morphology |
J:335489
|
absent heart right ventricle |
J:335489
|
enlarged heart |
J:335489
|
heart right ventricle hypoplasia |
J:335489
|
ventricular septal defect |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1a(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Sox10-cre)1Wdr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * CBA
|
normal
cardiovascular system phenotype |
J:335489
|
cleft chin |
J:335489
|
cleft palate |
J:335489
|
facial cleft |
J:335489
|
frontal bone hypoplasia |
J:335489
|
nasal bone hypoplasia |
J:335489
|
short mandible |
J:335489
|
temporal bone squamous part hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1a(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Wnt1-cre/Esr1*)10Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
decreased heart left ventricle wall thickness |
J:335489
|
embryonic lethality during organogenesis, complete penetrance |
J:335489
|
flat forehead |
J:335489
|
increased vascular permeability |
J:335489
|
lethality throughout fetal growth and development |
J:335489
|
persistent truncus arteriosus |
J:335489
|
pharyngeal arch artery hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1c(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Mef2c-cre)2Blk/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
abnormal heart right ventricle outflow tract morphology |
J:335489
|
absent heart right ventricle |
J:335489
|
enlarged heart |
J:335489
|
heart right ventricle hypoplasia |
J:335489
|
ventricular septal defect |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1c(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Sox10-cre)1Wdr/0
Not Specified
|
cardiovascular system phenotype |
J:335489
|
cleft chin |
J:335489
|
cleft palate |
J:335489
|
facial cleft |
J:335489
|
frontal bone hypoplasia |
J:335489
|
nasal bone hypoplasia |
J:335489
|
short mandible |
J:335489
|
temporal bone squamous part hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1c(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Wnt1-cre/Esr1*)10Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
decreased heart left ventricle wall thickness |
J:335489
|
embryonic lethality during organogenesis, complete penetrance |
J:335489
|
flat forehead |
J:335489
|
increased vascular permeability |
J:335489
|
lethality throughout fetal growth and development |
J:335489
|
persistent truncus arteriosus |
J:335489
|
pharyngeal arch artery hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu Tg(Sox10-cre)1Wdr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N * CBA
|
cleft palate |
J:335489
|
facial cleft |
J:335489
|
midline cleft upper lip |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu Tg(Wnt1-cre/Esr1*)10Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N
|
normal
cardiovascular system phenotype |
J:335489
|
facial cleft |
J:335489
|
flat forehead |
J:335489
|
lethality throughout fetal growth and development |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1d(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Mef2c-cre)2Blk/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
abnormal heart right ventricle outflow tract morphology |
J:335489
|
absent heart right ventricle |
J:335489
|
enlarged heart |
J:335489
|
heart right ventricle hypoplasia |
J:335489
|
ventricular septal defect |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1d(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Sox10-cre)1Wdr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * CBA
|
cardiovascular system phenotype |
J:335489
|
cleft chin |
J:335489
|
cleft palate |
J:335489
|
facial cleft |
J:335489
|
frontal bone hypoplasia |
J:335489
|
nasal bone hypoplasia |
J:335489
|
short mandible |
J:335489
|
temporal bone squamous part hypoplasia |
J:335489
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Polr1atm1d(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu Tg(Wnt1-cre/Esr1*)10Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
|
decreased heart left ventricle wall thickness |
J:335489
|
embryonic lethality during organogenesis, complete penetrance |
J:335489
|
flat forehead |
J:335489
|
increased vascular permeability |
J:335489
|
lethality throughout fetal growth and development |
J:335489
|
persistent truncus arteriosus |
J:335489
|
pharyngeal arch artery hypoplasia |
J:335489
|