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
N N
cardiovascular system phenotype
N N
abnormal lung vasculature morphology
abnormal placenta vasculature
vascular smooth muscle hypertrophy
heart right ventricle hypertrophy
increased right ventricle systolic pressure
pulmonary hypertension
hypertension
increased systemic arterial systolic blood pressure
increased vascular smooth muscle cell proliferation
cellular
increased vascular smooth muscle cell proliferation
increased hepatocyte karyomegaly
maternal effect
embryo
N
embryo phenotype
N
abnormal placenta morphology
abnormal placenta vasculature
small placenta
decreased placenta weight
endocrine/exocrine glands
abnormal thymus corticomedullary boundary morphology
small thymus
growth/size/body
heart right ventricle hypertrophy
decreased body weight
hematopoietic system
abnormal thymus corticomedullary boundary morphology
small thymus
increased double-negative T cell number
anemia
increased granulocyte number
increased eosinophil cell number
increased dendritic cell number
increased macrophage cell number
decreased leukocyte cell number
decreased T cell number
decreased double-positive T cell number
abnormal spleen red pulp morphology
small spleen
spleen hypoplasia
decreased immunoglobulin level
homeostasis/metabolism
decreased circulating serum albumin level
decreased circulating total protein level
cyanosis
abnormal enzyme/coenzyme level
increased urine protein level
abnormal nucleotide metabolism
immune system
abnormal thymus corticomedullary boundary morphology
small thymus
increased double-negative T cell number
increased granulocyte number
increased eosinophil cell number
increased dendritic cell number
increased macrophage cell number
decreased leukocyte cell number
decreased T cell number
decreased double-positive T cell number
abnormal spleen red pulp morphology
small spleen
spleen hypoplasia
decreased immunoglobulin level
abnormal dendritic cell physiology
lung inflammation
liver/biliary system
abnormal liver morphology
abnormal hepatocyte morphology
increased hepatocyte karyomegaly
decreased hepatocyte number
small liver
hepatic necrosis
mortality/aging
neonatal lethality, complete penetrance
postnatal lethality, complete penetrance
muscle
vascular smooth muscle hypertrophy
heart right ventricle hypertrophy
increased vascular smooth muscle cell proliferation
renal/urinary system
N
renal/urinary system phenotype
N N
increased urine protein level
abnormal renal glomerulus morphology
abnormal renal tubule morphology
reproductive system
abnormal penile erection
priapism
respiratory system
abnormal lung vasculature morphology
lung inflammation
abnormal pulmonary alveolar system morphology
increased lung elastance
increased airway resistance
tachypnea
decreased lung compliance
abnormal pulmonary gas exchange
skeleton
abnormal costochondral joint morphology
abnormal rib morphology
normal phenotype
no abnormal phenotype detected