Mouse (66 sources):
abnormal DNA replication,
abnormal alveolar macrophage morphology,
abnormal alveolar macrophage physiology,
abnormal atrium myocardium morphology,
abnormal blastocoele morphology,
abnormal blastocyst morphology,
abnormal cell morphology,
abnormal cerebellum deep nucleus morphology,
abnormal dorsal root ganglion morphology,
abnormal embryonic/fetal subventricular zone morphology,
abnormal endosome to melanosome transport,
abnormal enterocyte morphology,
abnormal hair follicle melanocyte morphology,
abnormal inner cell mass morphology,
abnormal lipid level,
abnormal locomotor behavior,
abnormal melanosome maturation,
abnormal pons morphology,
abnormal pulmonary alveolar system morphology,
abnormal renal tubule morphology,
abnormal small intestinal microvillus morphology,
abnormal thymus morphology,
abnormal trophectoderm morphology,
abnormal ventricle myocardium morphology,
abnormal visceral endoderm morphology,
abnormal visceral endoderm physiology,
absent blastocoele,
brain vacuoles,
decreased alveolar macrophage number,
decreased birth body size,
decreased brain weight,
decreased circulating free fatty acids level,
decreased embryo size,
decreased heart weight,
decreased muscle cell glucose uptake,
decreased regulatory T cell number,
decreased small intestinal microvillus size,
diluted coat color,
disheveled coat,
embryonic growth arrest,
embryonic lethality before implantation, complete penetrance,
embryonic lethality before implantation, incomplete penetrance,
embryonic lethality between somite formation and embryo turning, complete penetrance,
homeostasis/metabolism phenotype,
hunched posture,
immune system phenotype,
increased adipocyte glucose uptake,
increased gonadal fat pad weight,
increased interleukin-13 secretion,
increased interleukin-4 secretion,
increased renal fat pad weight,
increased susceptibility to age related obesity,
increased susceptibility to type I hypersensitivity reaction,
increased total body fat amount,
intestinal fibrosis,
kidney degeneration,
lethality, incomplete penetrance,
muscle phenotype,
no abnormal phenotype detected,
perinatal lethality, incomplete penetrance,
postnatal lethality, complete penetrance,
premature death,
prenatal lethality, incomplete penetrance,
pulmonary vascular congestion,
reduced hair shaft melanin granule number,
small heart
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