Mouse (149 sources):
abnormal adipose tissue amount,
abnormal angiogenesis,
abnormal body length,
abnormal bone mineralization,
abnormal branching of the mammary ductal tree,
abnormal cell morphology,
abnormal cell nucleus morphology,
abnormal chorion morphology,
abnormal chromosome number,
abnormal common myeloid progenitor cell morphology,
abnormal definitive hematopoiesis,
abnormal dorsal aorta morphology,
abnormal embryonic erythropoiesis,
abnormal embryo turning,
abnormal enterocyte physiology,
abnormal enterocyte proliferation,
abnormal fluid intake,
abnormal frontal bone morphology,
abnormal hematopoietic system morphology/development,
abnormal hepatocyte morphology,
abnormal immune system organ morphology,
abnormal intestinal enteroendocrine cell morphology,
abnormal intestinal goblet cell morphology,
abnormal involution of the mammary gland,
abnormal large intestine crypts of Lieberkuhn morphology,
abnormal liver lobule morphology,
abnormal liver sinusoid morphology,
abnormal lymphopoiesis,
abnormal malleus morphology,
abnormal mammary gland alveolus morphology,
abnormal mammary gland development,
abnormal mammary gland epithelium physiology,
abnormal mammary gland lobule morphology,
abnormal mammary gland morphology,
abnormal middle ear ossicle morphology,
abnormal mitosis,
abnormal pancreas development,
abnormal pancreatic acinar cell morphology,
abnormal pancreatic acinus morphology,
abnormal pancreatic duct morphology,
abnormal placenta morphology,
abnormal proerythroblast morphology,
abnormal response to injury,
abnormal skeletal muscle morphology,
abnormal small intestine crypts of Lieberkuhn morphology,
abnormal startle reflex,
abnormal T cell receptor beta chain V(D)J recombination,
abnormal trophoblast layer morphology,
abnormal vascular development,
abnormal vasculogenesis,
abnormal visceral yolk sac morphology,
absent common myeloid progenitor cells,
absent erythroid progenitor cell,
absent fibroblast proliferation,
absent pancreatic acinar cells,
absent pinna reflex,
aneuploidy,
belly spot,
binucleate,
cardiovascular system phenotype,
chromosomal instability,
decreased B cell proliferation,
decreased birth body size,
decreased birth weight,
decreased body size,
decreased bone marrow cell number,
decreased bone mineral content,
decreased cell proliferation,
decreased common myeloid progenitor cell number,
decreased embryo size,
decreased fetal size,
decreased fibroblast proliferation,
decreased fluid intake,
decreased hematocrit,
decreased litter size,
decreased liver glycogen level,
decreased memory T cell number,
decreased NK T cell number,
decreased pancreas weight,
decreased Paneth cell number,
decreased prepulse inhibition,
decreased small intestinal villus size,
decreased T cell proliferation,
decreased tumor incidence,
decreased white adipose tissue amount,
distended pericardium,
embryonic growth retardation,
embryonic lethality during organogenesis, complete penetrance,
endocrine/exocrine gland phenotype,
enlarged lymph nodes,
enlarged thymus,
exocrine pancreas atrophy,
focal hepatic necrosis,
immune system phenotype,
impaired hematopoiesis,
increased adenoma incidence,
increased B cell apoptosis,
increased B cell derived lymphoma incidence,
increased B cell proliferation,
increased circulating creatinine level,
increased hepatocellular carcinoma incidence,
increased hepatoma incidence,
increased liver adenoma incidence,
increased liver weight,
increased lymphoma incidence,
increased macrophage cell number,
increased mammary adenocarcinoma incidence,
increased mammary gland apoptosis,
increased mammary gland tumor incidence,
increased metastatic potential,
increased pancreatic acinar cell carcinoma incidence,
increased pituitary gland tumor incidence,
increased pre-B cell number,
increased spleen weight,
increased startle reflex,
increased T cell derived lymphoma incidence,
increased tumor incidence,
induced chromosome breakage,
lactation failure,
liver/biliary system phenotype,
liver hypoplasia,
liver vascular congestion,
lymphoid hypoplasia,
mammary gland alveolar hyperplasia,
mammary gland duct hyperplasia,
mammary gland hyperplasia,
microvesicular hepatic steatosis,
muscular atrophy,
neonatal lethality, incomplete penetrance,
no abnormal phenotype detected,
open neural tube,
pale yolk sac,
pancreatic islet hyperplasia,
placental labyrinth hypoplasia,
polyploidy,
postnatal lethality, complete penetrance,
premature death,
prenatal lethality, complete penetrance,
reduced female fertility,
short malleus manubrium,
short tail,
small cranium,
small liver,
small lymphoid organs,
small malleus,
small nasal bone,
small pancreas,
spleen hyperplasia,
spontaneous chromosome breakage
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