Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Phenotypes:
Affected Systems
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cardiovascular system
phlebitis
cellular
abnormal T cell proliferation
increased T cell proliferation
digestive/alimentary system
abnormal salivary gland morphology
salivary gland inflammation
endocrine/exocrine glands
abnormal salivary gland morphology
salivary gland inflammation
thymus hypoplasia
pancreas fibrosis
pancreas inflammation
growth/size/body
decreased body weight
enlarged spleen
increased spleen weight
spleen hyperplasia
hematopoietic system
abnormal T cell proliferation
increased T cell proliferation
thymus hypoplasia
enlarged spleen
increased spleen weight
spleen hyperplasia
increased susceptibility to autoimmune hemolytic anemia
increased eosinophil cell number
abnormal lymphocyte morphology
abnormal T cell selection
decreased double-positive T cell number
abnormal gamma-delta T cell differentiation
arrested T cell differentiation
increased B cell number
increased plasma cell number
abnormal T cell subpopulation ratio
absent CD4-positive, alpha-beta T cells
increased CD4-positive, alpha-beta T cell number
increased T-helper 2 cell number
absent CD8-positive, alpha-beta T cells
increased memory T cell number
decreased regulatory T cell number
increased spleen germinal center number
abnormal spleen periarteriolar lymphoid sheath morphology
abnormal B cell activation
increased IgE level
increased IgG1 level
increased IgM level
abnormal T-helper 2 physiology
abnormal regulatory T cell physiology
decreased platelet aggregation
abnormal platelet dense granule physiology
homeostasis/metabolism
decreased platelet aggregation
abnormal platelet dense granule physiology
increased blood urea nitrogen level
albuminuria
immune system
immune system phenotype
N N
abnormal T cell proliferation
increased T cell proliferation
increased susceptibility to autoimmune hemolytic anemia
abnormal B cell activation
abnormal T-helper 2 physiology
abnormal regulatory T cell physiology
abnormal immune system morphology
increased eosinophil cell number
abnormal lymphocyte morphology
abnormal T cell selection
decreased double-positive T cell number
abnormal gamma-delta T cell differentiation
arrested T cell differentiation
increased B cell number
increased plasma cell number
abnormal T cell subpopulation ratio
absent CD4-positive, alpha-beta T cells
increased CD4-positive, alpha-beta T cell number
increased T-helper 2 cell number
absent CD8-positive, alpha-beta T cells
increased memory T cell number
decreased regulatory T cell number
abnormal immune system organ morphology
thymus hypoplasia
enlarged spleen
increased spleen weight
spleen hyperplasia
increased spleen germinal center number
abnormal spleen periarteriolar lymphoid sheath morphology
abnormal lymph node secondary follicle morphology
abnormal lymph node germinal center morphology
enlarged lymph nodes
abnormal immune serum protein physiology
increased IgE level
increased IgG1 level
increased IgM level
increased interferon-gamma secretion
increased interleukin-4 secretion
increased anti-erythrocyte antigen antibody level
increased anti-nuclear antigen antibody level
increased anti-chromatin antibody level
chronic inflammation
increased inflammatory response
phlebitis
salivary gland inflammation
pancreas inflammation
liver inflammation
kidney inflammation
glomerulonephritis
lung inflammation
liver/biliary system
liver inflammation
renal/urinary system
albuminuria
kidney inflammation
glomerulonephritis
renal glomerular immunoglobulin deposits
renal fibrosis
respiratory system
lung inflammation