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Proper Citation: RRID:MGI:3589925
Description: Allele Detail: Spontaneous This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Spontaneous This is a legacy resource.
Phenotype: parakeratosis, abnormal epidermal layer morphology, blepharitis, abnormal B cell physiology, abnormal spleen B cell follicle morphology, abnormal hepatic cord morphology, hemosiderosis, abnormal lymph node medullary cord morphology, abnormal lymph node B cell domain morphology, pale kidney, enlarged liver, skin lesions, small ears, small testis, small thymus, thick ears, abnormal thymus morphology, abnormal macrophage morphology, enlarged heart, distended abdomen, dermatitis, decreased hemoglobin content, decreased hematocrit, cryptorchism, cachexia, anemia, abnormal atrial thrombosis, abnormal erythrocyte morphology, premature death, anisocytosis, decreased body size, scaly ears, scaly skin, abnormal thymus cortex morphology, enlarged lymph nodes, enlarged liver sinusoidal spaces, increased spleen weight, abnormal tail ring morphology, polychromatophilia, epidermal hyperplasia, hunched posture, extramedullary hematopoiesis, orthokeratosis, increased IgG level, abnormal spleen white pulp morphology, increased spleen red pulp amount, abnormal spleen morphology, absent spleen marginal zone, pleural effusion, increased IgM level, increased leukocyte cell number, increased inflammatory response, increased mean corpuscular volume, poikilocytosis, jaundice, abnormal male reproductive system morphology, abnormal lymphocyte morphology, liver inflammation, abnormal lymph node morphology, abnormal lymph node T cell domain morphology, abnormal liver morphology, multifocal hepatic necrosis
Affected Gene: Foxp3
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No rating or validation information has been found for Foxp3sf.
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Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI