Mouse (67 sources):
Purkinje cell degeneration,
abnormal Paneth cell morphology,
abnormal T cell subpopulation ratio,
abnormal adenohypophysis morphology,
abnormal amino acid level,
abnormal autophagy,
abnormal axon morphology,
abnormal cardiac muscle contractility,
abnormal cerebellar granule cell morphology,
abnormal cerebral cortex morphology,
abnormal circulating chemokine level,
abnormal hepatocyte morphology,
abnormal inferior colliculus morphology,
abnormal intestinal goblet cell morphology,
abnormal kidney morphology,
abnormal lysosome morphology,
abnormal macrophage physiology,
abnormal motor capabilities/coordination/movement,
abnormal myocardial fiber physiology,
abnormal proximal convoluted tubule morphology,
abnormal renal glomerulus morphology,
abnormal suckling behavior,
abnormal thymus cortex morphology,
absent gastric milk in neonates,
absent otoliths,
adipose tissue phenotype,
cellular phenotype,
decreased CD4-positive, alpha beta T cell number,
decreased T cell proliferation,
decreased a-wave amplitude,
decreased b-wave amplitude,
decreased cerebral cortex pyramidal cell number,
decreased circulating interleukin-10 level,
decreased grip strength,
dilated heart left ventricle,
enlarged myocardial fiber,
enlarged otoliths,
growth/size/body region phenotype,
hematopoietic system phenotype,
homeostasis/metabolism phenotype,
impaired autophagy,
increased anti-double stranded DNA antibody level,
increased anti-nuclear antigen antibody level,
increased autoantibody level,
increased circulating creatinine level,
increased circulating interleukin-1 beta level,
increased circulating interleukin-12b level,
increased circulating interleukin-6 level,
increased heart weight,
increased kidney weight,
increased lung weight,
increased mitochondrial size,
increased neutrophil cell number,
increased physiological sensitivity to xenobiotic,
increased sensitivity to induced morbidity/mortality,
increased susceptibility to systemic lupus erythematosus,
limb grasping,
neonatal lethality, complete penetrance,
nervous system phenotype,
neuron degeneration,
neuronal intranuclear inclusions,
no abnormal phenotype detected,
oxidative stress,
premature death,
short stride length,
valinuria,
vision/eye phenotype
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