Mouse (53 sources):
abnormal allantois morphology,
abnormal angiogenesis,
abnormal brain vasculature morphology,
abnormal cardiac outflow tract development,
abnormal cell migration,
abnormal developmental vascular remodeling,
abnormal direction of embryo turning,
abnormal direction of heart looping,
abnormal embryo development,
abnormal epidermal-dermal junction morphology,
abnormal fetal atrioventricular canal morphology,
abnormal gastrulation,
abnormal heart development,
abnormal heart echocardiography feature,
abnormal impulse conducting system conduction,
abnormal mesoderm development,
abnormal mycoardial fiber sodium currents,
abnormal myocardial fiber physiology,
abnormal placental labyrinth vasculature morphology,
abnormal primitive streak morphology,
abnormal sebocyte differentiation,
abnormal vascular branching morphogenesis,
abnormal vitelline vascular remodeling,
absent amnion,
absent chorion,
decreased angiogenesis,
decreased atrioventricular cushion size,
decreased body size,
decreased cardiac muscle contractility,
decreased embryo size,
decreased food intake,
decreased sensitivity to induced cell death,
dilated heart left ventricle,
dilated heart ventricle,
embryonic growth arrest,
embryonic growth retardation,
embryonic lethality between somite formation and embryo turning, complete penetrance,
embryonic lethality during organogenesis, complete penetrance,
embryonic lethality, complete penetrance,
flaky skin,
increased allantois apoptosis,
increased basal cell carcinoma incidence,
increased keratinocyte proliferation,
increased metastatic potential,
increased sebaceous gland tumor incidence,
increased skin tumor incidence,
no abnormal phenotype detected,
premature death,
prolonged QRS complex duration,
sebaceous gland hyperplasia,
short tail,
thin placenta labyrinth,
thin ventricular wall
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