Mouse (104 sources):
abnormal axon guidance,
abnormal blood coagulation,
abnormal CD4-positive, alpha beta T cell morphology,
abnormal CD8-positive, alpha-beta T cell number,
abnormal cochlea morphology,
abnormal cochlear ganglion morphology,
abnormal cochlear hair cell morphology,
abnormal cochlear outer hair cell morphology,
abnormal craniofacial bone morphology,
abnormal crista ampullaris morphology,
abnormal definitive hematopoiesis,
abnormal double-positive T cell morphology,
abnormal embryo development,
abnormal embryonic growth/weight/body size,
abnormal endolymphatic duct morphology,
abnormal epidermis stratum basale morphology,
abnormal hair cuticle,
abnormal hair cycle,
abnormal hair follicle inner root sheath morphology,
abnormal hair follicle melanin granule morphology,
abnormal hair follicle morphology,
abnormal hair follicle orientation,
abnormal hair follicle outer root sheath morphology,
abnormal hair shaft melanin granule distribution,
abnormal humoral immune response,
abnormal immune system organ morphology,
abnormal inner ear development,
abnormal mammary gland growth during lactation,
abnormal mesonephros morphology,
abnormal nervous system development,
abnormal organ of Corti morphology,
abnormal otic vesicle development,
abnormal pyloric sphincter morphology,
abnormal Raphe nucleus morphology,
abnormal sensory neuron innervation pattern,
abnormal skin condition,
abnormal stomach smooth muscle circular layer morphology,
abnormal stomach smooth muscle outer longitudinal layer morphology,
abnormal sympathetic ganglion morphology,
abnormal sympathetic neuron innervation pattern,
abnormal T cell differentiation,
abnormal T cell subpopulation ratio,
abnormal vestibular ganglion morphology,
abnormal vibrissa morphology,
abnormal Wolffian duct morphology,
absent cochlear hair cells,
absent common crus,
absent distortion product otoacoustic emissions,
absent ureteric bud,
absent utricle,
absent vestibular saccule,
absent Wolffian ducts,
arrested T cell differentiation,
cochlear ganglion degeneration,
cochlear hair cell degeneration,
cochlear inner hair cell degeneration,
cochlear outer hair cell degeneration,
curly vibrissae,
decreased body size,
decreased CD4-positive, alpha beta T cell number,
decreased cochlear hair cell number,
decreased double-negative T cell number,
decreased double-positive T cell number,
decreased eosinophil cell number,
decreased gamma-delta T cell number,
decreased interleukin-13 secretion,
decreased interleukin-4 secretion,
decreased organ of Corti supporting cell number,
decreased serotonin level,
decreased T-helper 2 cell number,
decreased thymocyte number,
degeneration of organ of Corti supporting cells,
delayed hair appearance,
delayed inner ear development,
embryonic lethality during organogenesis, complete penetrance,
endocrine/exocrine gland phenotype,
enlarged sebaceous gland,
epidermal hyperplasia,
focal dorsal hair loss,
impaired skin barrier function,
increased apoptosis,
increased interferon-gamma secretion,
increased or absent threshold for auditory brainstem response,
increased susceptibility to parasitic infection,
increased T cell apoptosis,
increased T-helper 1 cell number,
inner ear cyst,
inner ear hypoplasia,
lactation failure,
neonatal lethality, complete penetrance,
no abnormal phenotype detected,
organ of Corti degeneration,
pillar cell degeneration,
prenatal lethality,
prenatal lethality, incomplete penetrance,
progressive hair loss,
sensorineural hearing loss,
short hair,
short vibrissae,
small otic vesicle,
small superior cervical ganglion,
small thymus,
thick hair follicle outer root sheath,
thin dermal layer
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