124 phenotypes from 1 allele in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tgfb2tm1Doe/Tgfb2+ involves: 129/Sv * 129P2/OlaHsd * Black Swiss * C57BL/6J	decreased dopamine level	J:108007
	decreased dopaminergic neuron number	J:108007
Tgfb2tm1Doe/Tgfb2+ involves: 129P2/OlaHsd	abnormal small intestinal villus morphology	J:76342
	decreased enterocyte apoptosis	J:76342
Tgfb2tm1Doe/Tgfb2+ involves: 129P2/OlaHsd * Black Swiss	abnormal bulbourethral gland morphology	J:78547
	abnormal bulbourethral gland physiology	J:78547
	abnormal spermatogenesis	J:78547
	bulbourethral gland cyst	J:78547
	bulbourethral gland hyperplasia	J:78547
	oligozoospermia	J:78547
	prostate gland anterior lobe hyperplasia	J:78547
	teratozoospermia	J:78547
Tgfb2tm1Doe/Tgfb2+ STOCK Tgfb2tm1Doe/J	abnormal aorta wall morphology	J:188799
	aortic aneurysm	J:188799
	dilated aorta bulb	J:188799
Tgfb2tm1Doe/Tgfb2tm1Doe involves: 129P2/OlaHsd	normal limbs/digits/tail phenotype	J:76541
Tgfb2tm1Doe/Tgfb2tm1Doe involves: 129P2/OlaHsd * Black Swiss	aberrant origin of the right subclavian artery	J:103391
	abnormal aorta morphology	J:103391
	abnormal atrioventricular cushion morphology	J:103391
	abnormal atrioventricular valve morphology	J:41682, J:103391
	abnormal cardiac outflow tract development	J:103391
	abnormal cardiovascular development	J:103391
	abnormal clavicle morphology	J:41682
	abnormal cochlea morphology	J:41682
	abnormal cochlear ganglion morphology	J:41682
	abnormal cornea posterior stroma morphology	J:73681
	abnormal corneal stroma morphology	J:73681
	abnormal craniofacial bone morphology	J:41682
	abnormal eye posterior chamber morphology	J:41682
	abnormal femur morphology	J:41682
	abnormal heart septum morphology	J:103391
	abnormal heart ventricle outflow tract morphology	J:103391
	abnormal humerus morphology	J:41682
	abnormal iris stroma morphology	J:73681
	abnormal kidney morphology	J:41682
	abnormal limb morphology	J:41682
	abnormal macrophage physiology	J:73681
	abnormal mandible morphology	J:41682
	abnormal myocardium layer morphology	J:41682, J:103391
	abnormal neurocranium morphology	J:41682
	abnormal renal tubule epithelium morphology	J:41682
	abnormal retina neuronal layer morphology	J:73681
	abnormal rib morphology	J:41682
	abnormal scala vestibuli morphology	J:41682
	abnormal semilunar valve morphology	J:41682, J:103391
	abnormal sternum morphology	J:41682
	abnormal thoracic cage shape	J:41682
	abnormal trochanter morphology	J:41682
	abnormal truncus arteriosus septation	J:103391
	abnormal uterine horn morphology	J:41682
	abnormal xiphoid process morphology	J:41682
	absent alisphenoid bone	J:41682
	absent corneal endothelium	J:73681
	absent deltoid tuberosity	J:41682
	absent Descemet membrane	J:73681
	absent eye anterior chamber	J:73681
	absent interdental cells	J:41682
	absent kidney	J:41682
	absent mandibular angle	J:41682
	absent maxillary shelf	J:41682
	absent occipital bone	J:41682
	absent pterygoid process	J:41682
	absent Rosenthal canal	J:41682
	absent spiral limbus	J:41682
	aortic arch hypoplasia	J:103391
	ascending aorta hypoplasia	J:41682, J:103391
	atelectasis	J:41682
	atrioventricular septal defect	J:103391
	cleft secondary palate	J:41682
	complete atrioventricular septal defect	J:103391
	cyanosis	J:41682
	decreased body weight	J:41682
	decreased cornea thickness	J:73681
	decreased corneal stroma thickness	J:41682, J:73681
	dilated heart right ventricle	J:41682, J:103391
	dilated renal tubule	J:41682
	dilated respiratory conducting tube	J:41682
	double inlet heart left ventricle	J:41682
	double outlet right ventricle	J:41682, J:103391
	ectopic adrenal gland	J:41682
ectopic testis	J:41682
failure of atrioventricular cushion closure	J:103391
failure of heart looping	J:103391
failure of palatal shelf elevation	J:41682
fused cornea and lens	J:73681
heart valve hyperplasia	J:103391
hydronephrosis	J:41682
increased urine protein level	J:41682
inlet ventricular septal defect	J:41682, J:103391
interrupted aortic arch	J:103391
interrupted aortic arch, type b	J:103391
large fontanelles	J:41682
neonatal lethality, complete penetrance	J:41682, J:73681
ostium primum atrial septal defect	J:103391
patent aortic valve	J:41682
patent pulmonary valve	J:41682
perimembraneous ventricular septal defect	J:103391
perinatal lethality, incomplete penetrance	J:41682
persistence of hyaloid vascular system	J:73681
persistent right dorsal aorta	J:103391
pulmonary artery hypoplasia	J:103391
respiratory distress	J:41682
retina hyperplasia	J:41682
retrognathia	J:41682
rib fusion	J:41682
short mandible	J:41682
short radius	J:41682
short ulna	J:41682
small frontal bone	J:41682
small interparietal bone	J:41682
small mandibular condyloid process	J:41682
small mandibular coronoid process	J:41682
small olecranon	J:41682
small parietal bone	J:41682
small temporal bone	J:41682
spina bifida occulta	J:41682
testis hypoplasia	J:41682
thick aortic valve cusps	J:103391
thick mitral valve	J:103391
thick pulmonary valve cusps	J:103391
thick tricuspid valve	J:103391
trabecula carnea hypoplasia	J:41682
vitreous body deposition	J:73681
Tgfb2tm1Doe/Tgfb2tm1Doe involves: 129P2/OlaHsd * C57BL/6	primary vitreous hyperplasia	J:149526