Mouse (112 sources):
abnormal Langerhans cell morphology,
abnormal M line morphology,
abnormal T-helper 2 cell morphology,
abnormal Z line morphology,
abnormal atrioventricular cushion morphology,
abnormal atrioventricular valve morphology,
abnormal cardiac thrombosis,
abnormal cone electrophysiology,
abnormal conotruncal ridge morphology,
abnormal conotruncus septation,
abnormal corneal stroma morphology,
abnormal dendritic cell physiology,
abnormal epidermis stratum corneum morphology,
abnormal extraembryonic tissue morphology,
abnormal eye development,
abnormal hair cycle anagen phase,
abnormal hair cycle telogen phase,
abnormal hair follicle melanin granule distribution,
abnormal hair follicle morphology,
abnormal heart development,
abnormal keratinocyte morphology,
abnormal kidney morphology,
abnormal macrophage activation involved in immune response,
abnormal melanosome morphology,
abnormal mitral valve morphology,
abnormal myocardial fiber morphology,
abnormal myocardium compact layer morphology,
abnormal myocardium layer morphology,
abnormal nephron morphology,
abnormal pericardial cavity morphology,
abnormal pericardium morphology,
abnormal peritoneal macrophage morphology,
abnormal pharyngeal arch artery morphology,
abnormal photoreceptor outer segment morphology,
abnormal piliary canal morphology,
abnormal placenta labyrinth morphology,
abnormal placenta morphology,
abnormal podocyte foot process morphology,
abnormal postnatal growth/weight/body size,
abnormal prostate gland branching morphogenesis,
abnormal prostate gland physiology,
abnormal regulatory T cell physiology,
abnormal renal glomerulus morphology,
abnormal respiratory electron transport chain,
abnormal retina outer nuclear layer morphology,
abnormal retina pigment epithelium morphology,
abnormal rod electrophysiology,
abnormal sarcomere morphology,
abnormal skeleton development,
abnormal skin condition,
abnormal truncus arteriosus septation,
abnormal vasculogenesis,
abnormal ventricle papillary muscle morphology,
absent Harderian gland,
absent sclera,
absent sublingual duct,
behavior/neurological phenotype,
decreased cardiac output,
decreased fetal size,
decreased hepatocyte proliferation,
decreased retina photoreceptor cell number,
decreased ventral retina size,
decreased ventricle muscle contractility,
delayed dark adaptation,
delayed hair appearance,
delayed hepatic development,
dermal cyst,
dilated heart atrium,
dilated piliary canal,
diluted coat color,
disorganized outer root sheath cells,
disorganized photoreceptor outer segment,
distorted hair follicle pattern,
failure of atrioventricular cushion closure,
fused podocyte foot processes,
hair follicle degeneration,
impaired macrophage phagocytosis,
increased anti-double stranded DNA antibody level,
increased anti-nuclear antigen antibody level,
increased anti-single stranded DNA antibody level,
increased autoantibody level,
increased circulating creatine level,
increased keratinocyte proliferation,
increased kidney weight,
increased mesangial cell number,
increased prostate intraepithelial neoplasia incidence,
increased renal glomerulus apoptosis,
increased renal glomerulus basement membrane thickness,
lethality throughout fetal growth and development, complete penetrance,
lethality throughout fetal growth and development, incomplete penetrance,
myocardial fiber degeneration,
no abnormal phenotype detected,
perinatal lethality, complete penetrance,
postnatal lethality, incomplete penetrance,
premature death,
prenatal lethality,
prostate gland epithelial hyperplasia,
renal glomerulus hypertrophy,
retina pigment epithelium atrophy,
shiny skin,
short photoreceptor outer segment,
skin edema,
skin lesions,
small liver,
thick dermal layer,
thick epidermis suprabasal layer,
thin hypodermis,
thin ventricular wall,
trabecula carnea hypoplasia,
ventral rotation of lens,
ventricular hypoplasia,
ventricular myocardium compact layer hypoplasia
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