Mouse (81 sources):
abnormal apoptosis,
abnormal brain development,
abnormal brain ventricle morphology,
abnormal cerebral hemisphere morphology,
abnormal cortical marginal zone morphology,
abnormal cranial flexure morphology,
abnormal craniofacial bone morphology,
abnormal craniofacial morphology,
abnormal cranium morphology,
abnormal embryonic neuroepithelial layer differentiation,
abnormal embryonic neuroepithelium morphology,
abnormal embryonic tissue morphology,
abnormal embryonic/fetal subventricular zone morphology,
abnormal fibroblast apoptosis,
abnormal folding of telencephalic vesicles,
abnormal forebrain development,
abnormal forehead shape,
abnormal fourth ventricle morphology,
abnormal frontal bone morphology,
abnormal lens polarity,
abnormal maxilla morphology,
abnormal nasal septum morphology,
abnormal neurocranium morphology,
abnormal neuron differentiation,
abnormal neuron physiology,
abnormal otic vesicle development,
abnormal palate morphology,
abnormal presphenoid bone morphology,
abnormal respiratory electron transport chain,
abnormal retina neuronal layer morphology,
abnormal seminiferous tubule morphology,
abnormal spermatogonia morphology,
abnormal telencephalon morphology,
abnormal third ventricle morphology,
abnormal viscerocranium morphology,
absent ethmoid bone,
absent interparietal bone,
absent neurocranium,
absent parietal bone,
absent presphenoid bone,
absent supraoccipital bone,
absent vomer bone,
broad frontonasal prominence,
choroid plexus hyperplasia,
cranioschisis,
curly tail,
decreased apoptosis,
decreased fibroblast apoptosis,
decreased neuron apoptosis,
decreased sensitivity to induced cell death,
decreased survivor rate,
delayed neural tube closure,
diencephalon hyperplasia,
failure of eyelid fusion,
hearing/vestibular/ear phenotype,
hypothalamus hyperplasia,
immune system phenotype,
impaired ossification of basisphenoid bone,
increased cell proliferation,
increased embryonic neuroepithelium thickness,
increased neuron apoptosis,
interdigital webbing,
kinked tail,
lethality throughout fetal growth and development, complete penetrance,
lethality throughout fetal growth and development, incomplete penetrance,
midbrain hyperplasia,
nervous system phenotype,
no abnormal phenotype detected,
open neural tube,
perinatal lethality, complete penetrance,
perinatal lethality, incomplete penetrance,
persistence of hyaloid vascular system,
persistence of medial edge epithelium during palatal shelf fusion,
postnatal lethality, complete penetrance,
postnatal lethality, incomplete penetrance,
premature death,
reduced female fertility,
reduced male fertility,
retina hyperplasia,
small embryonic telencephalon,
thalamus hyperplasia
[+]
|