Myh10b2b2437Clo/Myh10b2b2437Clo
C57BL/6J-Myh10b2b2437Clo
|
abnormal cranium morphology |
J:175213
|
|
abnormal myocardium compact layer morphology |
J:175213
|
|
atrioventricular septal defect |
J:175213
|
|
cleft upper lip |
J:175213
|
|
double outlet right ventricle |
J:175213
|
|
double outlet right ventricle with atrioventricular septal defect |
J:175213
|
|
exencephaly |
J:175213
|
|
micrognathia |
J:175213
|
|
overriding aortic valve |
J:175213
|
|
ventricular septal defect |
J:175213
|
Myh10ehc/Myh10ehc
involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6J
|
abnormal heart apex morphology |
J:248868
|
|
abnormal heart atrium morphology |
J:248868
|
|
abnormal heart ventricle morphology |
J:248868
|
|
abnormal myocardium compact layer morphology |
J:248868
|
|
abnormal ventricle myocardium morphology |
J:248868
|
|
absent coronary vessels |
J:248868
|
|
domed cranium |
J:248868
|
|
double outlet right ventricle |
J:248868
|
|
edema |
J:248868
|
|
heart hemorrhage |
J:248868
|
|
hemopericardium |
J:248868
|
|
hydrocephaly |
J:248868
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:248868
|
|
myocardial trabeculae hypoplasia |
J:248868
|
|
pericardial effusion |
J:248868
|
|
thin interventricular septum |
J:248868
|
|
ventricular septal defect |
J:248868
|
Myh10ehc/Myh10tm2Rsad
involves: 129S4/SvJae * 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6J
|
abnormal heart morphology |
J:248868
|
|
abnormal myocardium compact layer morphology |
J:248868
|
|
absent coronary vessels |
J:248868
|
|
embryonic lethality, complete penetrance |
J:248868
|
Myh10em1(IMPC)J/Myh10+
C57BL/6NJ-Myh10em1(IMPC)J/J
|
increased fasting circulating glucose level |
J:211773
|
Myh10em1(IMPC)J/Myh10em1(IMPC)J
C57BL/6NJ-Myh10em1(IMPC)J/J
|
abnormal pericardium morphology |
J:211773
|
|
abnormal placenta size |
J:211773
|
|
abnormal skin coloration |
J:211773
|
|
edema |
J:211773
|
|
embryonic growth retardation |
J:211773
|
|
hemorrhage |
J:211773
|
|
prenatal lethality prior to heart atrial septation |
J:211773
|
|
preweaning lethality, complete penetrance |
J:211773
|
Myh10tm1Rsad/Myh10tm1Rsad
involves: 129S4/SvJae
|
cardiac hypertrophy |
J:92230
|
Myh10tm1Rsad/Myh10tm2Rsad
involves: 129S4/SvJae
|
cardiac hypertrophy |
J:92230
|
Myh10tm2Rsad/Myh10+
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6
|
normal
growth/size/body region phenotype |
J:245570
|
Myh10tm2Rsad/Myh10tm2Rsad
involves: 129S4/SvJae
|
abnormal fetal cardiomyocyte morphology |
J:92230
|
|
abnormal heart morphology |
J:248868
|
|
abnormal myocardium compact layer morphology |
J:248868
|
|
abnormal spinal cord morphology |
J:124610
|
|
absent coronary vessels |
J:248868
|
|
normal
cardiovascular system phenotype |
J:248868
|
|
decreased fetal cardiomyocyte number |
J:92230
|
|
decreased fetal cardiomyocyte proliferation |
J:92230
|
|
hydrocephaly |
J:124610
|
|
increased cardiomyocyte apoptosis |
J:248868
|
|
increased fetal cardiomyocyte size |
J:92230
|
|
thin ventricular wall |
J:92230
|
Myh10tm2Rsad/Myh10tm2Rsad
involves: 129S4/SvJae * C57BL/6
|
abnormal atrioventricular valve development |
J:245570
|
|
abnormal cardiac outflow tract development |
J:245570
|
|
abnormal fetal cardiomyocyte morphology |
J:168304
|
|
abnormal fourth ventricle morphology |
J:112536
|
|
decreased fetal cardiomyocyte number |
J:168304
|
|
double outlet right ventricle |
J:245570
|
|
normal
growth/size/body region phenotype |
J:245570
|
|
hydrocephaly |
J:112536
|
Myh10tm2Rsad/Myh10tm2Rsad
involves: 129S4/SvJae * C57BL/6J
|
abnormal aortic valve morphology |
J:44181
|
|
abnormal birth body size |
J:44181
|
|
abnormal fetal cardiomyocyte morphology |
J:44181
|
|
abnormal liver morphology |
J:44181
|
|
abnormal retina morphology |
J:44181
|
|
abnormal suckling behavior |
J:44181
|
|
absent retina bipolar cells |
J:44181
|
|
congestive heart failure |
J:44181
|
|
dilated heart right atrium |
J:44181
|
|
domed cranium |
J:44181
|
|
fetal cardiomyocyte disarray |
J:44181
|
|
globular heart |
J:44181
|
|
heart right ventricle outflow tract stenosis |
J:44181
|
|
hydrocephaly |
J:44181
|
|
increased fetal cardiomyocyte size |
J:44181
|
|
liver vascular congestion |
J:44181
|
|
neonatal lethality, complete penetrance |
J:44181
|
|
overriding aortic valve |
J:44181
|
|
perimembraneous ventricular septal defect |
J:44181
|
|
prenatal lethality, incomplete penetrance |
J:44181
|
Myh10tm2Rsad/Myh10tm3.1Rsad
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6
|
failure of ventral body wall closure |
J:245570
|
Myh10tm2Rsad/Myh10tm4Rsad
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6
|
abnormal fourth ventricle morphology |
J:112536
|
|
hydrocephaly |
J:112536
|
Myh10tm2Rsad/Myh10tm5Rsad
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6
|
abnormal fourth ventricle morphology |
J:112536
|
|
hydrocephaly |
J:112536
|
Myh10tm3.1Rsad/Myh10+
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6
|
failure of ventral body wall closure |
J:245570
|
Myh10tm3.1Rsad/Myh10+
involves: 129S6/SvEvTac * BALB/c * C57BL/6
|
abnormal diaphragm development |
J:245570
|
|
normal
cardiovascular system phenotype |
J:245570
|
|
diaphragmatic hernia |
J:245570
|
|
herniated liver |
J:245570
|
|
omphalocele |
J:245570
|
|
thin diaphragm muscle |
J:245570
|
Myh10tm3.1Rsad/Myh10tm3.1Rsad
involves: 129S6/SvEvTac * BALB/c * C57BL/6
|
abnormal atrioventricular valve development |
J:245570
|
|
abnormal cardiac outflow tract development |
J:245570
|
|
abnormal conotruncal ridge morphology |
J:245570
|
|
abnormal diaphragm development |
J:245570
|
|
abnormal sternum morphology |
J:245570
|
|
cleft palate |
J:245570
|
|
congestive heart failure |
J:245570
|
|
decreased apoptosis |
J:245570
|
|
decreased cardiac muscle contractility |
J:245570
|
|
decreased heart rate |
J:245570
|
|
decreased palatal shelf size |
J:245570
|
|
diaphragmatic hernia |
J:245570
|
|
dilated liver sinusoidal space |
J:245570
|
|
double outlet right ventricle |
J:245570
|
|
ectopia cordis |
J:245570
|
|
failure of atrioventricular cushion closure |
J:245570
|
|
failure of palatal shelf elevation |
J:245570
|
|
failure of ventral body wall closure |
J:245570
|
|
generalized edema |
J:245570
|
|
herniated liver |
J:245570
|
|
increased heart left ventricle size |
J:245570
|
|
lethality throughout fetal growth and development, complete penetrance |
J:92081,
J:245570
|
|
liver hemorrhage |
J:245570
|
|
liver vascular congestion |
J:245570
|
|
omphalocele |
J:245570
|
|
split sternum |
J:245570
|
|
umbilical hernia |
J:245570
|
Myh10tm3Rsad/Myh10tm3Rsad
involves: 129S6/SvEvTac * C57BL/6
|
abnormal cerebellar foliation |
J:92081
|
|
abnormal cerebellar granule layer morphology |
J:92081
|
|
abnormal cerebellar molecular layer |
J:92081
|
|
abnormal cerebellum external granule cell layer morphology |
J:92081
|
|
abnormal cerebellum morphology |
J:92081
|
|
abnormal cerebral cortex morphology |
J:92081
|
|
abnormal facial nerve morphology |
J:92081
|
|
abnormal fourth ventricle morphology |
J:112536
|
|
abnormal heart ventricle morphology |
J:92230
|
|
abnormal neuronal migration |
J:92081
|
|
abnormal Purkinje cell morphology |
J:92081
|
|
ataxia |
J:92081
|
|
decreased Purkinje cell size |
J:92081
|
|
normal
growth/size/body region phenotype |
J:245570
|
|
hydrocephaly |
J:92081,
J:112536
|
|
impaired balance |
J:92081
|
|
postnatal lethality, complete penetrance |
J:92081
|
|
small cerebellum |
J:92081
|
Myh10tm4Rsad/Myh10tm4Rsad
involves: 129S6/SvEvTac * C57BL/6
|
abnormal cerebral aqueduct morphology |
J:168304
|
|
abnormal fourth ventricle morphology |
J:112536
|
|
abnormal myocardial fiber physiology |
J:168304
|
|
abnormal neuronal migration |
J:112536
|
|
dilated brain ventricle |
J:112536
|
|
dilated lateral ventricle |
J:112536
|
|
dilated third ventricle |
J:112536
|
|
hydrocephaly |
J:112536
|
|
postnatal lethality, incomplete penetrance |
J:112536
|
Myh10tm5Rsad/Myh10tm5Rsad
involves: 129S6/SvEvTac * C57BL/6
|
abnormal cerebellar Purkinje cell layer |
J:112536
|
|
abnormal Purkinje cell dendrite morphology |
J:112536
|
|
ectopic Purkinje cell |
J:112536
|
|
impaired coordination |
J:112536
|
|
normal
nervous system phenotype |
J:112536
|
Myh10tm5Rsad/Myh10tm5Rsad
Tg(CMV-cre)1Cgn/0
involves: 129S6/SvEvTac * BALB/cJ * C57BL/6
|
abnormal cerebellar Purkinje cell layer |
J:112536
|
|
abnormal Purkinje cell dendrite morphology |
J:112536
|
|
ectopic Purkinje cell |
J:112536
|
|
impaired coordination |
J:112536
|
Myh10tm7Rsad/Myh10tm7Rsad
Tg(Myh6-cre)2182Mds/0
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
|
abnormal atrial thrombosis |
J:170148
|
|
abnormal impulse conducting system conduction |
J:170148
|
|
abnormal intercalated disk morphology |
J:170148
|
|
cardiac interstitial fibrosis |
J:170148
|
|
cardiomyopathy |
J:170148
|
|
decreased cardiac muscle contractility |
J:170148
|
|
heart inflammation |
J:170148
|
|
increased cardiomyocyte apoptosis |
J:170148
|
|
increased myocardial fiber size |
J:170148
|
|
ventricular septal defect |
J:170148
|
Myh10tm7Rsad/Myh10tm7Rsad
Tg(Nes-cre)1Wme/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA
|
abnormal cerebellum development |
J:170148
|
|
abnormal locomotor behavior |
J:170148
|
|
abnormal spinal cord central canal morphology |
J:170148
|
|
normal
cardiovascular system phenotype |
J:170148
|
|
enlarged lateral ventricles |
J:170148
|
|
hydrocephaly |
J:170148
|
|
postnatal lethality, complete penetrance |
J:170148
|
|
thin cerebral cortex |
J:170148
|
Myh10tm8Rsad/Myh10tm8Rsad
involves: 129
|
no abnormal phenotype detected |
J:124610
|
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